US20180085150A1 - Methods and apparatus for treating vertebral fractures - Google Patents

Methods and apparatus for treating vertebral fractures Download PDF

Info

Publication number
US20180085150A1
US20180085150A1 US15/728,581 US201715728581A US2018085150A1 US 20180085150 A1 US20180085150 A1 US 20180085150A1 US 201715728581 A US201715728581 A US 201715728581A US 2018085150 A1 US2018085150 A1 US 2018085150A1
Authority
US
United States
Prior art keywords
shaft
balloon
balloon implant
cavity
vertebral body
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US15/728,581
Inventor
Damien O'Halloran
David C. Paul
Sean Suh
Stephen Cicchini
Robert Doran
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Globus Medical Inc
Original Assignee
Globus Medical Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Globus Medical Inc filed Critical Globus Medical Inc
Priority to US15/728,581 priority Critical patent/US20180085150A1/en
Assigned to GLOBUS MEDICAL, INC. reassignment GLOBUS MEDICAL, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: PAUL, DAVID C., SUH, SEAN, CICCHINI, STEPHEN, DORAN, ROBERT, O'HALLORAN, DAMIEN
Publication of US20180085150A1 publication Critical patent/US20180085150A1/en
Priority to EP18199049.0A priority patent/EP3470000A1/en
Priority to JP2018191439A priority patent/JP2019069151A/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/70Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
    • A61B17/7097Stabilisers comprising fluid filler in an implant, e.g. balloon; devices for inserting or filling such implants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/70Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
    • A61B17/7094Solid vertebral fillers; devices for inserting such fillers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/88Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
    • A61B17/8802Equipment for handling bone cement or other fluid fillers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/88Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
    • A61B17/8802Equipment for handling bone cement or other fluid fillers
    • A61B17/8805Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it
    • A61B17/8811Equipment for handling bone cement or other fluid fillers for introducing fluid filler into bone or extracting it characterised by the introducer tip, i.e. the part inserted into or onto the bone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/88Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
    • A61B17/885Tools for expanding or compacting bones or discs or cavities therein
    • A61B17/8852Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc
    • A61B17/8855Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc inflatable, e.g. kyphoplasty balloons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B2017/564Methods for bone or joint treatment

Definitions

  • the present disclosure generally relates to treatment of bones.
  • the present disclosure relates to methods and apparatus for treatment of vertebral fractures that include an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment.
  • Bones and bony structures are susceptible to a variety of weaknesses that can affect their ability to provide support and structure. Weaknesses in bony structures may have many causes, including degenerative diseases, tumors, fractures, and dislocations. By way of example, weaknesses in vertebrae from lead to compression fractures that involve the collapse of one or more vertebrae in the spine. These vertebral compression fractures may be caused by a number of conditions including osteoporosis, trauma, and tumors. Advances in medicine and engineering have provided doctors with a plurality of devices and techniques for alleviating or curing these weaknesses.
  • vertebroplasty One technique for treating vertebral fractures is vertebroplasty.
  • a physician may use a needle to inject bone cement into a fractured vertebral body to stabilize the fracture.
  • Kyphoplasty is another technique for treating vertebra fractures that involves insertion of a balloon into the fractured vertebra to create a bone cavity in the vertebra. The balloon may then be removed followed by injection of bone cement into the vertebral body to stabilize the fracture. Leakage of the bone cement in both vertebroplasty and kyphoplasty is a common problem that can lead to complications. Another problem associated with these techniques is the potential for inadequate height restoration to the fractured vertebral body.
  • the present disclosure generally relates to treatment of bones.
  • the present disclosure relates to methods and apparatus for treatment of vertebral fractures that includes a device for cavity creation, an inflation device and a containment device for maintaining vertebral height and cement containment.
  • An embodiment of the present invention includes a method for treating a bone.
  • the method may comprise creating a cavity in the bone.
  • the method further may comprise placing a containment jacket in the cavity.
  • the method further may comprise inflating a balloon within the containment jacket so that the balloon occupies a first portion of the containment jacket.
  • the method further may comprise introducing a first filler material into a second portion of the containment jacket, wherein the second portion of the containment jacket is not occupied by the balloon.
  • the method further may comprise removing the balloon from the containment jacket.
  • the method further may comprise introducing a second filler material into the first portion of the containment jacket.
  • FIG. 1 is a cross-sectional view of a vertebral body in accordance with one embodiment of the present technique.
  • FIG. 2 illustrates an inflation device inserted into a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 3 illustrates employment of an inflation device to create a cavity in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 4 illustrates a cavity created in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 5 illustrates employment of an inflation and containment device in a. vertebral body in accordance with one embodiment of the present invention.
  • FIG. 6 illustrates further employment of an inflation and containment device in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 7 illustrates a stabilized vertebral body in accordance with one embodiment of the present invention.
  • FIG. 8 illustrates a containment jacket in accordance with one embodiment of the present invention.
  • FIG. 9 is a close-up view of a containment jacket in accordance with one embodiment of the present invention.
  • FIGS. 10 and 11 illustrate an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 12 illustrates employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 13 illustrates further employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 14 illustrates yet further employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIGS. 15-21 illustrate yet another embodiment of a system and method for treating vertebral fractures.
  • FIGS. 22A-29 illustrate another embodiment of a system for treating vertebral fractures.
  • the present disclosure generally relates to treatment of bones.
  • the present disclosure relates to methods and apparatus for treatment of vertebral fractures that include an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment.
  • FIG. 1 illustrates a vertebral body 10 having a compression fracture therein with associated loss of height.
  • the vertebral body 10 includes an exterior portion of cortical bone 12 and an interior portion of cancellous bone 14 .
  • FIGS. 2-4 illustrate creation of a cavity in the vertebral body 10 , in accordance with one embodiment of the present invention.
  • an inflation device 16 may be inserted into the cancellous bone 14 of the vertebral body 10 .
  • the inflation device 16 includes a fill tube 18 and a first balloon 20 on the distal end of the fill tube 18 .
  • the first balloon 20 may be deflated when the inflation device 16 is inserted into the vertebral body 10 .
  • the inflation device 16 may be an inflatable bone tamp. It should be understood that the passageway into the vertebral body 10 for the inflation device 16 may be created using any of a variety of different suitable techniques.
  • a trocar may be used to place a cannula into the patient's body.
  • a drill may then be inserted into the cannula, for example, and used to create a channel into the vertebral body 10 into which the inflation device 16 may be inserted.
  • the inflation device 16 may then be inserted through the cannula into the vertebral body 10 , for example.
  • FIG. 3 illustrates employment of the inflation device 16 to create a cavity 22 in the vertebral body 10 , in accordance with one embodiment of the present invention.
  • the first balloon 20 may inflate, for example, to compact the cancellous bone 14 in the interior portion of the vertebral body 10 .
  • the first balloon 20 may also, for example, force apart the compact bone 12 , restoring height to the vertebral body 10 .
  • the inflation device 16 may then be removed from the vertebral body 10 .
  • FIG. 3 illustrates the use of the first balloon 2 . 0 for creation of the cavity 22
  • an expandable jack or other suitable device may be used to create the cavity 22 in the vertebral body 10 .
  • FIG. 4 illustrates the cavity 22 that has been created in the vertebral body 10 after removal of the inflation device 16 , in accordance with embodiments of the present invention. While not illustrated, embodiments of the present invention further may include coating the wall of the cavity 22 with a bone growing agent, or a hemostatic sealing agent.
  • FIG. 5 illustrates employment of an inflation and containment device 24 in the vertebral body, in accordance with embodiments of the present invention.
  • the inflation and containment device 24 may be inserted into the cavity 22 in the vertebral body 10 .
  • a second inflation device may be inserted into the vertebral body 10 through a cannula (not illustrated).
  • the inflation and containment device 24 includes an exterior tube 26 , an interior fill tube 28 , a second balloon 30 , and a containment jacket 32 .
  • the second balloon 30 may be employed to maintain the height of the vertebral body 10 while the cavity 22 is partially filled with a first volume 34 of a filler material.
  • the containment jacket 32 may be employed to contain a filler material (e.g., cement) introduced into the cavity 22 to prevent undesirable leakage, In this manner, problems associated with leakage of the filler material from the cavity 22 and loss of vertebral height may be reduced or possibly even avoided.
  • a filler material e.g., cement
  • the second balloon 30 may be located on a distal end or proximal end of the interior fill tube 28 , in accordance with embodiments of the present invention.
  • the second balloon 30 and interior fill tube 28 may be an inflatable bone tamp.
  • the second balloon 30 is deflated when the inflation and containment device 24 is inserted into the vertebral body 10 . After insertion into the cavity 22 , the second balloon 30 may then be inflated.
  • inflation of the second balloon 30 should provide pressure on the walls of the cavity 22 to prevent (or reduce) loss of vertebral height. It may be desirable, in certain embodiments, for expansion of the second balloon 30 to further increase the height of the vertebral body 10 .
  • inflation of the second balloon 30 may restore some vertebral height lost after removal of the first balloon 20 .
  • the second balloon 30 generally may be enclosed within the containment jacket 32 .
  • the volume of the second balloon 30 generally should be smaller than the volume of the containment jacket 32 , in accordance with embodiments of the present invention.
  • the second balloon 30 when inflated, generally should not occupy the entire volume of the containment jacket 32 .
  • the second balloon 30 may occupy from about 10% to about 90% by volume of the containment jacket 32 .
  • the containment jacket 32 may be located on a distal end of the exterior tube 26 , in accordance with embodiments of the present invention. As illustrated, the containment jacket 32 may be attached to the distal end of the exterior tube 26 such that the containment jacket 32 encloses the distal end of the exterior tube 26 . While not illustrated, the containment jacket 32 may be deflated when the inflation and containment device 24 is inserted into the vertebral body 10 . After insertion into the cavity 22 , the containment jacket 32 may be inflated as the second balloon within the containment jacket is inflated. As illustrated, the containment jacket 32 may conform to the shape of the cavity 22 . In certain embodiments, the volume of the containment jacket 32 may be larger than the volume of the cavity 22 .
  • the containment jacket 32 may be a compliant balloon (e.g., polyurethane) that can contain the filler material to prevent leakage. Accordingly, the containment jacket may permit interdigitation of the filler material with the cancellous bone, in accordance with embodiments of the present invention.
  • a compliant balloon e.g., polyurethane
  • employment of the inflation and containment device 24 includes inflation of the containment jacket 32 and inflation of the second balloon 30 , in accordance with embodiments of the present technique.
  • the cavity 22 may then be partially filled with a first cement volume 34 .
  • the first cement volume 34 may be introduced into the containment jacket 32 , for example, by way of the exterior tube 26 .
  • the first cement volume 34 generally may fill the portion of the containment jacket 32 that is not occupied by the inflated second balloon 30 .
  • the first cement volume 34 may occupy from about 10% to about 90% by volume of the containment jacket 32 as inflated in the cavity 22 .
  • the first cement volume 34 may then be allowed to cure in the containment jacket 32 .
  • the second balloon 30 may be removed from the cavity.
  • FIG. 6 illustrates further employment of the inflation and containment device 24 in accordance with embodiments of the present invention.
  • the second balloon 30 may be removed from the cavity 22 after the first cement volume 34 has substantially cured.
  • the containment jacket 32 remains in the cavity 22 .
  • a second cement volume 36 may then be introduced into the containment jacket 32 .
  • the second cement volume 36 generally may occupy the unoccupied portion of the containment jacket 32 , for example, the portion of the containment, jacket 32 that is not occupied by the first volume 32 of cement.
  • the second cement volume 36 may occupy from about 10% to about 90% by volume of the containment jacket 32 as inflated in the cavity 22 .
  • the second cement volume 36 may then be allowed to cure in the containment jacket 32 .
  • the inflation and containment device 24 may then be removed from the vertebral body 10 .
  • the containment jacket 32 may be detached from the device 24 and remain in the vertebral body 10 .
  • FIG. 7 illustrates the vertebral body 10 after stabilization of the compression fracture therein in accordance with embodiments of the present invention.
  • the containment jacket 32 remains in the vertebral body 10 generally filling the cavity 22 .
  • the first cement volume 34 and the second cement volume 36 generally fill the containment jacket 32 .
  • height may be restored to the vertebral body 10 in accordance with embodiments of the present invention.
  • FIGS. 5-7 describes the use of the inflation and containment device 24
  • the inflation and containment device 24 is an illustration of one device for maintaining vertebral height and cement containment in accordance with embodiments of the present technique.
  • Other suitable devices for maintaining vertebral height and cement containment may also be used in present embodiments.
  • FIGS. 8-9 illustrate the containment jacket 32 in accordance with one embodiment of the present invention.
  • FIG. 9 is a close-up view of the containment jacket 32 in accordance with one embodiment of the present invention.
  • the outer surface of the containment jacket 32 may be coated with a bone growing agent.
  • the bone growing agent may be any of a variety of different materials suitable for promoting growth of the cancellous bone 14 that is adjacent to the containment jacket 32 in the vertebral body 10 .
  • FIGS. 10-11 illustrate an inflation and containment device 24 that may be used in accordance with one embodiment of the present invention.
  • the device 24 may be inserted into a vertebral body 10 .
  • the inflation and containment device 24 may comprise an exterior tube 26 , an interior fill tube 28 , a second balloon 30 in a deflated state, and a containment jacket 32 .
  • the exterior tube 26 is a dual-duct tube that comprises an exterior passageway 40 an interior passageway 42 .
  • the exterior passageway may surround the interior passageway 42 with the passageways separated by an interior wall 43 .
  • Both the exterior passageway 40 and the interior passageway 42 may, for example, extend along the longitudinal axis 44 of the exterior tube.
  • the distal end 46 of the exterior tube 26 may include one or more exit ports 48 for the exterior passageway 40 .
  • the exit ports 48 may be spaced around the interior passageway 42 .
  • the interior passageway 42 may be used to deliver, example, the first cement volume 34 into the containment jacket 32 .
  • the interior fill tube 28 may be disposed through the interior passageway 42 of the exterior tube 26 .
  • FIG. 12 illustrates employment of the inflation and containment device 24 in accordance with one embodiment of the present invention.
  • employment of the device 24 may comprise inflating the second balloon 30 and the containment jacket 32 .
  • Embodiments of the present invention further may comprise introduction of a first cement volume 34 into the containment jacket 32 .
  • the first cement volume 34 may be introduced into the volume of the containment jacket 34 that is not occupied by the second balloon.
  • the first cement volume 34 may be introduced through the exterior passageway 40 of the exterior tube 26 , exiting into the containment jacket 34 from the one or more exit ports 48 .
  • a sufficient amount of the first cement volume 34 may be introduced to generally fill the unoccupied portion of the containment jacket 34 .
  • the first cement volume 34 may then be allowed to cure in the containment jacket 34 .
  • FIG. 13 illustrates further employment of the inflation and containment device 24 in accordance with one embodiment of the present invention.
  • the second balloon 30 may be deflated and removed from the containment jacket 32 .
  • employment of the device 24 further may comprise introduction of the second cement volume 36 into the containment jacket 32 .
  • the second cement volume 36 may be introduced into the space within the containment jacket 32 that was previously occupied by the second balloon 30 in an inflated state.
  • a cement filling tube may be used to deliver the second cement volume 36 to the containment jacket 34 .
  • a sufficient amount of the second cement volume 36 may be introduced to substantially fill the remainder of the containment jacket 32 .
  • the second cement volume 36 may then be allowed to cure in the containment jacket 34 .
  • FIG. 14 illustrates yet further employment of the inflation and containment device 24 in accordance with one embodiment of the present invention.
  • the first cement volume 34 and the second cement volume 36 generally fill the containment jacket 32 .
  • the containment jacket 32 contains the cement volumes preventing undesirable leakage.
  • the exterior tube 26 may then be detached from the containment jacket 32 , leaving the containment jacket 32 in place. It should be noted that accessing the vertebral body may be achieved through the use of a cannula or through an open access method.
  • first cement volume 34 and a second cement volume 36 may comprise any of a variety of bone cements suitable for use in orthopedic applications.
  • An example of a suitable bone cement comprises polymethyl methacrylate (PMMA).
  • PMMA polymethyl methacrylate
  • embodiments of the present invention also may encompass a variety of different filler materials that may be utilized to, for example, fill and stabilize the cavity 22 in the vertebral body 10 . Examples of suitable materials may include human bone graft and synthetic derived bone substitutes.
  • a first balloon is used to create a cavity in the vertebral body.
  • any device that can be used to create cavity may be applied.
  • mechanical devices such as stents, drills, and vacuums may be used to create a cavity in the vertebral body.
  • a containment jacket and the second balloon can be introduced according to the present invention.
  • various different methods of deploying the second balloon within the containment jacket may be used.
  • the second balloon may be positioned in any position to maximize the efficiency and ease for inserting the cement into a particular position in the vertebral cavity.
  • FIGS. 15-21 illustrate a containment jacket 50 attached to a distal end of an insertion device 52 .
  • the insertion device 52 is adapted to be coupled to the containment jacket 50 .
  • the insertion device 52 is also provided with a central port 54 that is used to insert medical devices in the cavity of the vertebral body and is contained within the containment jacket 50 .
  • the central port 54 can be used to insert a k-wire, endoscopic devices, bone cement and other medically compatible instrument to enhance the procedure of curing bone cement within the vertebral cavity.
  • multiple balloons 56 may be attached. In different embodiments, the multiple balloons 56 may vary in size and shape.
  • sealing elements 57 are utilized to eliminate any risk of bone filler material or any other material being withdrawn through the insertion device 52 .
  • a central guide wire 58 is used to initially insert the containment jacket 50 within the vertebral body. Once the containment jacket 50 is positioned within the vertebral body as illustrated in FIG. 16 , the multiple balloons 56 are inserted into the cavity and inflated as illustrated in FIGS. 16 and 17 . As the balloons 56 are inflated, the pressure from the outer walls of the balloons 56 inflate the containment jacket 50 . After the balloons 56 are inflated to a volume that is optimal, a first filler material 60 is then inserted through the central port to a first portion within the containment jacket 50 . The balloons 56 are then deflated and removed from the containment jacket through the central port. Turning now to FIGS.
  • the first filler material 60 is cured, thereby providing stability and restoring height to one portion of the of the containment jacket within the vertebral body.
  • a second filler material 62 may be inserted into a second portion and allowed to cure within the containment jacket 50 , as shown in FIG. 20 .
  • FIG. 21 illustrates the first and second filler material being contained within the containment jacket 50 .
  • the containment jacket 50 conforms to the shape of the surrounding cancellous bone and interdigitates with the surrounding bone without any leakage of the first or second filler material.
  • a cavity creation balloon and a height restoration balloon may be configured within a containment jacket attached to a vertebral body insertion device.
  • containment jacket, the cavity creation balloon and the height restoration balloon are inserted into a fractured vertebral body.
  • the cavity creation balloon and the height restoration balloon are inflated simultaneous, thereby inflating the containment jacket within the vertebral body.
  • the cavity creation balloon is deflated and removed.
  • a bone filler material insertion device is inserted into the containment jacket and filled with a bone filler material in a first portion of the containment jacket.
  • the height restoration balloon is removed and a second bone filler material is inserted into the second portion of the containment jacket, Next, the second bone filler material is cured and the insertion devices are removed, leaving the containment jacket containing the first and second bone filler material in the vertebral body.
  • the preceding description is directed, for example, to treatment of vertebral fractures that includes an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment. It should be understood that the present technique also may be used in other suitable bone treatments were maintenance of vertebral height and/or cement containment may be desired. By way of example, embodiments of the present invention may be used to treat tibia plateau fractures, distal radius fractures, and cancellous fractures.
  • FIGS. 22A-29 illustrate an embodiment consistent with the principles of the present disclosure.
  • Implantable device 2200 may comprise a biocompatible balloon implant which can be inserted into a cavity of a vertebral body through a cannulated access system. After insertion, the balloon may be filled with bone cement and conform to the boundaries of the cavity. Implantable device 2200 may lower the chance of cement extravasation by containing the bone cement within itself.
  • the balloon implant which may be attached to a shaft of implantable device 2200 , can be detached after the cement cures, which leaves only the cement filled balloon in the vertebral body.
  • FIG. 22A illustrates an implantable device 2200 consistent with the principles of the present disclosure.
  • Implantable device 2200 may include a balloon implant 2202 , a shaft 2204 , a hub 2206 , and insertion mandrel 2208 .
  • Insertion mandrel 2208 may function to add rigidity to implantable device 2200 during insertion into the cavity. After insertion, balloon implant 2202 may be filled with bone cement.
  • implantable device 2200 is provided with a filler needle 2209 through which bone cement may be introduced into balloon implant 2202 .
  • FIG. 22C illustrates another view of filler needle 2209 being inserted into balloon implant 2202 .
  • Implantable balloon 2202 may be physically attached to shaft 2204 or implantable balloon 2202 and shaft 2204 may comprise a single unitary component.
  • Bone cement may be provided through filler needle 2209 to fill balloon 2202 .
  • filler needle 2209 may be placed through shaft 2204 to balloon implant 2202 allowing deposition of bone cement.
  • Filler needle 2209 may have laser markings on the outside to aid in determining the correct depth for injecting bone cement.
  • the diameter of filler needle 2209 may be determined such that the outside diameter of filler needle 2209 may have a clearance in relation to the inside diameter of shaft 2204 to allow for the venting of air, but not viscous liquids. This may aid in allowing for balloon implant 2202 to void entirely of air while being filled with bone cement.
  • Hub 2206 is shown in greater detail in FIG. 28 .
  • Hub 2206 may lock onto an access cannula 2210 , which may have a handle 2210 . This configuration may prevent rotation or axial movement of the implantable device 2200 .
  • wings 2214 of hub 2206 overlap handle 2210 and detents on hub 2206 may securely hold hub 2206 to handle 2210 .
  • FIG. 23 illustrates balloon implant 2202 rigidly attached to shaft 2204 .
  • a neck 2216 of balloon implant 2202 may be bonded to shaft 2204 .
  • Detachment of balloon implant 2202 from shaft 2204 is detailed with respect to FIGS. 26A-27 .
  • FIGS. 26A and 26B illustrate a detachment device 2600 , which may include jaws 2602 .
  • Detachment device 2600 may be a cannulated shaft, having multiple jaws 2602 , that is inserted into shaft 2204 and extends to neck 2216 .
  • a mandrel may be inserted into the detachment device 2600 through its cannulation and force jaws 2602 to expand, as shown in FIG. 27 .
  • FIG. 27 illustrates balloon implant 2202 , neck 2216 , cannula 2210 , jaws 2602 of device 2600 , and mandrel 2604 .
  • jaws 2602 Upon insertion of mandrel 2604 through the cannulation of the detachment device 2600 , jaws 2602 are forced to expand outwards towards the inner surface of cannula 2210 , which interferes with the surface. Because of this, jaws 2602 cut through neck 2216 of balloon implant 2602 and detachment device 2600 is rotated to fully sever neck 2216 and allow it and balloon implant 2202 to remain in the vertebral body.
  • balloon implant 2202 may be releasably attached to shaft 2204 .
  • shaft 2204 may comprise two steel tubes 2218 .
  • Balloon implant 2202 may be disposed in a manner such that neck 2216 may be tightly sandwiched between steel tubes 2218 .
  • one of steel tubes 2218 may be retracted thereby detaching balloon implant 2202 from shaft 2204 .
  • FIG. 25 illustrates another manner in which balloon implant 2202 may be released from shaft 2204 .
  • Neck 2216 may be engaged with shaft 2204 through a threaded connection.
  • a user may rotate shaft 2204 until the threaded connection is undone thereby detaching balloon implant 2202 from shaft 2204 .
  • FIG. 29 illustrates a method 2900 for delivering bone cement to a vertebral body consistent with the present disclosure.
  • a working cannula and introducer is used to access the desired vertebral body.
  • a scraper, curette, bone tamp, or any combination of the aforementioned may be used with fluoroscopic guidance to create a cavity within the cancellous bone of the vertebral body.
  • the cavity size may correspond to the size of the balloon implant being used.
  • the implant size may be designed to be larger than the cavity created such that the implant balloon does not stretch during cement filling.
  • the user may insert the inflation device through the cannula.
  • bone cement is first prepared by mixing the liquid and powder components. The cement may be injected though a filler needle. The filler delivery needle may be inserted through the shaft of the inflation device, into the balloon implant under fluoroscopic guidance.
  • the balloon implant may be separated through detachment, unthreading, or separation and left to remain within the vertebral body.

Landscapes

  • Health & Medical Sciences (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Medical Informatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Surgical Instruments (AREA)
  • Prostheses (AREA)

Abstract

Methods and apparatus for treating bones, including, in one or more embodiments, methods and apparatus for treatment of vertebral fractures that include an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment. Methods for treating a bone comprising: creating a cavity in the bone; inflating a containment jacket in the cavity; inflating a balloon within the containment jacket so that the balloon occupies a first portion of the containment jacket; introducing a first filler material into a second portion of the containment jacket, wherein the second portion of the containment jacket is not occupied by the balloon; removing the balloon from the containment jacket; and introducing a second filler material into the first portion of the containment jacket.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation-in-part application of U.S. patent application Ser. No. 15/355,100, filed on Nov. 18, 2016 (published as U.S. Patent Publication No. 2017-0065309), which is a continuation of U.S. patent application Ser. No. 14/254,614, filed on Apr. 16, 2014 (now issued as U.S. Pat. No. 9,526,550), which is a continuation of U.S. patent application Ser. No. 12/632,325, filed on Dec. 7, 2009 (now issued as U.S. Pat. No. 8,734,458), all of which are incorporated by reference in their entirety herein.
  • FIELD OF THE INVENTION
  • The present disclosure generally relates to treatment of bones. In particular, in one or more embodiments, the present disclosure relates to methods and apparatus for treatment of vertebral fractures that include an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment.
  • BACKGROUND
  • Bones and bony structures are susceptible to a variety of weaknesses that can affect their ability to provide support and structure. Weaknesses in bony structures may have many causes, including degenerative diseases, tumors, fractures, and dislocations. By way of example, weaknesses in vertebrae from lead to compression fractures that involve the collapse of one or more vertebrae in the spine. These vertebral compression fractures may be caused by a number of conditions including osteoporosis, trauma, and tumors. Advances in medicine and engineering have provided doctors with a plurality of devices and techniques for alleviating or curing these weaknesses.
  • One technique for treating vertebral fractures is vertebroplasty. In vertebroplasty, a physician may use a needle to inject bone cement into a fractured vertebral body to stabilize the fracture. Kyphoplasty is another technique for treating vertebra fractures that involves insertion of a balloon into the fractured vertebra to create a bone cavity in the vertebra. The balloon may then be removed followed by injection of bone cement into the vertebral body to stabilize the fracture. Leakage of the bone cement in both vertebroplasty and kyphoplasty is a common problem that can lead to complications. Another problem associated with these techniques is the potential for inadequate height restoration to the fractured vertebral body.
  • Thus, there is a need for methods and apparatus that can provide stabilization to a fractured vertebra.
  • SUMMARY
  • The present disclosure generally relates to treatment of bones. In particular, in one or more embodiments, the present disclosure relates to methods and apparatus for treatment of vertebral fractures that includes a device for cavity creation, an inflation device and a containment device for maintaining vertebral height and cement containment.
  • An embodiment of the present invention includes a method for treating a bone. The method may comprise creating a cavity in the bone. The method further may comprise placing a containment jacket in the cavity. The method further may comprise inflating a balloon within the containment jacket so that the balloon occupies a first portion of the containment jacket. The method further may comprise introducing a first filler material into a second portion of the containment jacket, wherein the second portion of the containment jacket is not occupied by the balloon. The method further may comprise removing the balloon from the containment jacket. The method further may comprise introducing a second filler material into the first portion of the containment jacket.
  • The features and advantages of the present invention will be readily apparent to those skilled in the art. While numerous changes may be made by those skilled in the art, such changes are within the spirit of the invention.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a cross-sectional view of a vertebral body in accordance with one embodiment of the present technique.
  • FIG. 2 illustrates an inflation device inserted into a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 3 illustrates employment of an inflation device to create a cavity in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 4 illustrates a cavity created in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 5 illustrates employment of an inflation and containment device in a. vertebral body in accordance with one embodiment of the present invention.
  • FIG. 6 illustrates further employment of an inflation and containment device in a vertebral body in accordance with one embodiment of the present invention.
  • FIG. 7 illustrates a stabilized vertebral body in accordance with one embodiment of the present invention.
  • FIG. 8 illustrates a containment jacket in accordance with one embodiment of the present invention.
  • FIG. 9 is a close-up view of a containment jacket in accordance with one embodiment of the present invention.
  • FIGS. 10 and 11 illustrate an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 12 illustrates employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 13 illustrates further employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIG. 14 illustrates yet further employment of an inflation and containment device in accordance with one embodiment of the present invention.
  • FIGS. 15-21 illustrate yet another embodiment of a system and method for treating vertebral fractures.
  • FIGS. 22A-29 illustrate another embodiment of a system for treating vertebral fractures.
  • DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS
  • The present disclosure generally relates to treatment of bones. In particular, in one or more embodiments, the present disclosure relates to methods and apparatus for treatment of vertebral fractures that include an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment.
  • FIG. 1 illustrates a vertebral body 10 having a compression fracture therein with associated loss of height. As illustrated, the vertebral body 10 includes an exterior portion of cortical bone 12 and an interior portion of cancellous bone 14.
  • FIGS. 2-4 illustrate creation of a cavity in the vertebral body 10, in accordance with one embodiment of the present invention. As illustrated in FIG. 2, an inflation device 16 may be inserted into the cancellous bone 14 of the vertebral body 10, In the illustrated embodiment, the inflation device 16 includes a fill tube 18 and a first balloon 20 on the distal end of the fill tube 18. As illustrated, the first balloon 20 may be deflated when the inflation device 16 is inserted into the vertebral body 10. In certain embodiments, the inflation device 16 may be an inflatable bone tamp. It should be understood that the passageway into the vertebral body 10 for the inflation device 16 may be created using any of a variety of different suitable techniques. While not illustrated, a trocar, for example, may be used to place a cannula into the patient's body. A drill may then be inserted into the cannula, for example, and used to create a channel into the vertebral body 10 into which the inflation device 16 may be inserted. The inflation device 16 may then be inserted through the cannula into the vertebral body 10, for example.
  • FIG. 3 illustrates employment of the inflation device 16 to create a cavity 22 in the vertebral body 10, in accordance with one embodiment of the present invention. As illustrated, the first balloon 20 may inflate, for example, to compact the cancellous bone 14 in the interior portion of the vertebral body 10. In addition to creation of the cavity 22, the first balloon 20 may also, for example, force apart the compact bone 12, restoring height to the vertebral body 10. The inflation device 16 may then be removed from the vertebral body 10. While FIG. 3 illustrates the use of the first balloon 2.0 for creation of the cavity 22, those of ordinary skill in the art will appreciate that other suitable techniques may also be used for creation of the cavity 22. By way of example, an expandable jack or other suitable device may be used to create the cavity 22 in the vertebral body 10.
  • FIG. 4 illustrates the cavity 22 that has been created in the vertebral body 10 after removal of the inflation device 16, in accordance with embodiments of the present invention. While not illustrated, embodiments of the present invention further may include coating the wall of the cavity 22 with a bone growing agent, or a hemostatic sealing agent.
  • FIG. 5 illustrates employment of an inflation and containment device 24 in the vertebral body, in accordance with embodiments of the present invention. As illustrated, the inflation and containment device 24 may be inserted into the cavity 22 in the vertebral body 10. In certain embodiments, a second inflation device may be inserted into the vertebral body 10 through a cannula (not illustrated). In the illustrated embodiment, the inflation and containment device 24 includes an exterior tube 26, an interior fill tube 28, a second balloon 30, and a containment jacket 32. As will be discussed in more detail below, the second balloon 30 may be employed to maintain the height of the vertebral body 10 while the cavity 22 is partially filled with a first volume 34 of a filler material. The containment jacket 32 may be employed to contain a filler material (e.g., cement) introduced into the cavity 22 to prevent undesirable leakage, In this manner, problems associated with leakage of the filler material from the cavity 22 and loss of vertebral height may be reduced or possibly even avoided.
  • The second balloon 30 may be located on a distal end or proximal end of the interior fill tube 28, in accordance with embodiments of the present invention. In certain embodiments, the second balloon 30 and interior fill tube 28 may be an inflatable bone tamp. While not illustrated, the second balloon 30 is deflated when the inflation and containment device 24 is inserted into the vertebral body 10. After insertion into the cavity 22, the second balloon 30 may then be inflated. In general, inflation of the second balloon 30 should provide pressure on the walls of the cavity 22 to prevent (or reduce) loss of vertebral height. It may be desirable, in certain embodiments, for expansion of the second balloon 30 to further increase the height of the vertebral body 10. In certain embodiments, inflation of the second balloon 30 may restore some vertebral height lost after removal of the first balloon 20. As illustrated, the second balloon 30 generally may be enclosed within the containment jacket 32. The volume of the second balloon 30 generally should be smaller than the volume of the containment jacket 32, in accordance with embodiments of the present invention. Furthermore, when inflated, the second balloon 30 generally should not occupy the entire volume of the containment jacket 32. By way of example, the second balloon 30 may occupy from about 10% to about 90% by volume of the containment jacket 32.
  • The containment jacket 32. may be located on a distal end of the exterior tube 26, in accordance with embodiments of the present invention. As illustrated, the containment jacket 32 may be attached to the distal end of the exterior tube 26 such that the containment jacket 32 encloses the distal end of the exterior tube 26. While not illustrated, the containment jacket 32 may be deflated when the inflation and containment device 24 is inserted into the vertebral body 10. After insertion into the cavity 22, the containment jacket 32 may be inflated as the second balloon within the containment jacket is inflated. As illustrated, the containment jacket 32 may conform to the shape of the cavity 22. In certain embodiments, the volume of the containment jacket 32 may be larger than the volume of the cavity 22. It may be desirable, in certain embodiments, for the containment jacket 32 to be a compliant balloon (e.g., polyurethane) that can contain the filler material to prevent leakage. Accordingly, the containment jacket may permit interdigitation of the filler material with the cancellous bone, in accordance with embodiments of the present invention.
  • As illustrated by FIG. 5, employment of the inflation and containment device 24 includes inflation of the containment jacket 32 and inflation of the second balloon 30, in accordance with embodiments of the present technique. As further illustrated by FIG. 5, the cavity 22 may then be partially filled with a first cement volume 34. In the illustrated embodiment, the first cement volume 34 may be introduced into the containment jacket 32, for example, by way of the exterior tube 26. The first cement volume 34 generally may fill the portion of the containment jacket 32 that is not occupied by the inflated second balloon 30. By way of example, the first cement volume 34 may occupy from about 10% to about 90% by volume of the containment jacket 32 as inflated in the cavity 22. The first cement volume 34 may then be allowed to cure in the containment jacket 32. After the first cement volume 34 has substantially cured, the second balloon 30 may be removed from the cavity.
  • FIG. 6 illustrates further employment of the inflation and containment device 24 in accordance with embodiments of the present invention. As previously mentioned, the second balloon 30 may be removed from the cavity 22 after the first cement volume 34 has substantially cured. In the illustrated embodiment, the containment jacket 32 remains in the cavity 22. As illustrated, a second cement volume 36 may then be introduced into the containment jacket 32. The second cement volume 36 generally may occupy the unoccupied portion of the containment jacket 32, for example, the portion of the containment, jacket 32 that is not occupied by the first volume 32 of cement. By way of example, the second cement volume 36 may occupy from about 10% to about 90% by volume of the containment jacket 32 as inflated in the cavity 22. The second cement volume 36 may then be allowed to cure in the containment jacket 32. The inflation and containment device 24 may then be removed from the vertebral body 10. In accordance with embodiments of the present invention, the containment jacket 32 may be detached from the device 24 and remain in the vertebral body 10.
  • FIG. 7 illustrates the vertebral body 10 after stabilization of the compression fracture therein in accordance with embodiments of the present invention. As illustrated, the containment jacket 32 remains in the vertebral body 10 generally filling the cavity 22. The first cement volume 34 and the second cement volume 36 generally fill the containment jacket 32. As is readily apparent from a comparison of FIG. 7 and FIG. 1, height may be restored to the vertebral body 10 in accordance with embodiments of the present invention.
  • While the preceding description of FIGS. 5-7 describes the use of the inflation and containment device 24, it should be understood that the inflation and containment device 24 is an illustration of one device for maintaining vertebral height and cement containment in accordance with embodiments of the present technique. Other suitable devices for maintaining vertebral height and cement containment may also be used in present embodiments.
  • FIGS. 8-9 illustrate the containment jacket 32 in accordance with one embodiment of the present invention. FIG. 9 is a close-up view of the containment jacket 32 in accordance with one embodiment of the present invention. As illustrated, the outer surface of the containment jacket 32 may be coated with a bone growing agent. The bone growing agent may be any of a variety of different materials suitable for promoting growth of the cancellous bone 14 that is adjacent to the containment jacket 32 in the vertebral body 10.
  • FIGS. 10-11 illustrate an inflation and containment device 24 that may be used in accordance with one embodiment of the present invention. As previously mentioned, the device 24 may be inserted into a vertebral body 10. As illustrated, the inflation and containment device 24 may comprise an exterior tube 26, an interior fill tube 28, a second balloon 30 in a deflated state, and a containment jacket 32, In the illustrated embodiment, the exterior tube 26 is a dual-duct tube that comprises an exterior passageway 40 an interior passageway 42. The exterior passageway may surround the interior passageway 42 with the passageways separated by an interior wall 43. Both the exterior passageway 40 and the interior passageway 42 may, for example, extend along the longitudinal axis 44 of the exterior tube. As illustrated, the distal end 46 of the exterior tube 26 may include one or more exit ports 48 for the exterior passageway 40. The exit ports 48 may be spaced around the interior passageway 42. The interior passageway 42 may be used to deliver, example, the first cement volume 34 into the containment jacket 32. The interior fill tube 28 may be disposed through the interior passageway 42 of the exterior tube 26.
  • FIG. 12 illustrates employment of the inflation and containment device 24 in accordance with one embodiment of the present invention. As illustrated, employment of the device 24 may comprise inflating the second balloon 30 and the containment jacket 32. Embodiments of the present invention further may comprise introduction of a first cement volume 34 into the containment jacket 32. As illustrated, the first cement volume 34 may be introduced into the volume of the containment jacket 34 that is not occupied by the second balloon. The first cement volume 34 may be introduced through the exterior passageway 40 of the exterior tube 26, exiting into the containment jacket 34 from the one or more exit ports 48. A sufficient amount of the first cement volume 34, for example, may be introduced to generally fill the unoccupied portion of the containment jacket 34. The first cement volume 34 may then be allowed to cure in the containment jacket 34.
  • FIG. 13 illustrates further employment of the inflation and containment device 24 in accordance with one embodiment of the present invention. After the first cement volume 34 is substantially cured, for example, the second balloon 30 may be deflated and removed from the containment jacket 32. As illustrated, employment of the device 24 further may comprise introduction of the second cement volume 36 into the containment jacket 32. By way of example, the second cement volume 36 may be introduced into the space within the containment jacket 32 that was previously occupied by the second balloon 30 in an inflated state. A cement filling tube may be used to deliver the second cement volume 36 to the containment jacket 34. In certain embodiments, a sufficient amount of the second cement volume 36 may be introduced to substantially fill the remainder of the containment jacket 32. The second cement volume 36 may then be allowed to cure in the containment jacket 34.
  • FIG. 14 illustrates yet further employment of the inflation and containment device 24 in accordance with one embodiment of the present invention. As illustrated, the first cement volume 34 and the second cement volume 36 generally fill the containment jacket 32. As previously mentioned, the containment jacket 32 contains the cement volumes preventing undesirable leakage. The exterior tube 26 may then be detached from the containment jacket 32, leaving the containment jacket 32 in place. It should be noted that accessing the vertebral body may be achieved through the use of a cannula or through an open access method.
  • The preceding description describes the use of a first cement volume 34 and a second cement volume 36 in accordance with embodiments of the present invention. Those of ordinary skill in the art will appreciate that the first cement volume 34 and the second cement volume 36 may comprise any of a variety of bone cements suitable for use in orthopedic applications. An example of a suitable bone cement comprises polymethyl methacrylate (PMMA). In addition, while the preceding description describes the use of cement, embodiments of the present invention also may encompass a variety of different filler materials that may be utilized to, for example, fill and stabilize the cavity 22 in the vertebral body 10. Examples of suitable materials may include human bone graft and synthetic derived bone substitutes.
  • In the exemplary embodiment, a first balloon is used to create a cavity in the vertebral body. However, any device that can be used to create cavity may be applied. For example, mechanical devices such as stents, drills, and vacuums may be used to create a cavity in the vertebral body. After the cavity is created, a containment jacket and the second balloon can be introduced according to the present invention. It should also be noted that various different methods of deploying the second balloon within the containment jacket may be used. For instance, the second balloon may be positioned in any position to maximize the efficiency and ease for inserting the cement into a particular position in the vertebral cavity.
  • In another exemplary embodiment of the present invention, FIGS. 15-21 illustrate a containment jacket 50 attached to a distal end of an insertion device 52. The insertion device 52 is adapted to be coupled to the containment jacket 50. The insertion device 52 is also provided with a central port 54 that is used to insert medical devices in the cavity of the vertebral body and is contained within the containment jacket 50. For instance, the central port 54 can be used to insert a k-wire, endoscopic devices, bone cement and other medically compatible instrument to enhance the procedure of curing bone cement within the vertebral cavity. On opposing sides of the central port 54 and at the distal end of the central port 54, multiple balloons 56 may be attached. In different embodiments, the multiple balloons 56 may vary in size and shape. Also, on opposing sides of the central port 54 and between the insertion device walls 52, there is provided sealing elements 57. The sealing elements 57 are utilized to eliminate any risk of bone filler material or any other material being withdrawn through the insertion device 52.
  • A central guide wire 58 is used to initially insert the containment jacket 50 within the vertebral body. Once the containment jacket 50 is positioned within the vertebral body as illustrated in FIG. 16, the multiple balloons 56 are inserted into the cavity and inflated as illustrated in FIGS. 16 and 17. As the balloons 56 are inflated, the pressure from the outer walls of the balloons 56 inflate the containment jacket 50. After the balloons 56 are inflated to a volume that is optimal, a first filler material 60 is then inserted through the central port to a first portion within the containment jacket 50. The balloons 56 are then deflated and removed from the containment jacket through the central port. Turning now to FIGS. 18 and 19, after removal of the balloons 56, the first filler material 60 is cured, thereby providing stability and restoring height to one portion of the of the containment jacket within the vertebral body. Once the first filler material 60 is cured, a second filler material 62 may be inserted into a second portion and allowed to cure within the containment jacket 50, as shown in FIG. 20. FIG. 21 illustrates the first and second filler material being contained within the containment jacket 50. Also, the containment jacket 50 conforms to the shape of the surrounding cancellous bone and interdigitates with the surrounding bone without any leakage of the first or second filler material.
  • In another embodiment of the present invention, a cavity creation balloon and a height restoration balloon may be configured within a containment jacket attached to a vertebral body insertion device. In one step of the present invention, containment jacket, the cavity creation balloon and the height restoration balloon are inserted into a fractured vertebral body. Next, the cavity creation balloon and the height restoration balloon are inflated simultaneous, thereby inflating the containment jacket within the vertebral body. Once the cavity is created and the height restoration balloon is inflated, the cavity creation balloon is deflated and removed. After removal of the cavity creation balloon, a bone filler material insertion device is inserted into the containment jacket and filled with a bone filler material in a first portion of the containment jacket. Once the bone filler material is cured, the height restoration balloon is removed and a second bone filler material is inserted into the second portion of the containment jacket, Next, the second bone filler material is cured and the insertion devices are removed, leaving the containment jacket containing the first and second bone filler material in the vertebral body.
  • In addition, the preceding description is directed, for example, to treatment of vertebral fractures that includes an inflation device for cavity creation and an inflation and containment device for maintaining vertebral height and cement containment. It should be understood that the present technique also may be used in other suitable bone treatments were maintenance of vertebral height and/or cement containment may be desired. By way of example, embodiments of the present invention may be used to treat tibia plateau fractures, distal radius fractures, and cancellous fractures.
  • FIGS. 22A-29 illustrate an embodiment consistent with the principles of the present disclosure. Implantable device 2200, as described in further detail below, may comprise a biocompatible balloon implant which can be inserted into a cavity of a vertebral body through a cannulated access system. After insertion, the balloon may be filled with bone cement and conform to the boundaries of the cavity. Implantable device 2200 may lower the chance of cement extravasation by containing the bone cement within itself. The balloon implant, which may be attached to a shaft of implantable device 2200, can be detached after the cement cures, which leaves only the cement filled balloon in the vertebral body.
  • FIG. 22A illustrates an implantable device 2200 consistent with the principles of the present disclosure. Implantable device 2200 may include a balloon implant 2202, a shaft 2204, a hub 2206, and insertion mandrel 2208. Insertion mandrel 2208 may function to add rigidity to implantable device 2200 during insertion into the cavity. After insertion, balloon implant 2202 may be filled with bone cement.
  • As shown in FIG. 22B, implantable device 2200 is provided with a filler needle 2209 through which bone cement may be introduced into balloon implant 2202. FIG. 22C illustrates another view of filler needle 2209 being inserted into balloon implant 2202. Implantable balloon 2202 may be physically attached to shaft 2204 or implantable balloon 2202 and shaft 2204 may comprise a single unitary component. Bone cement may be provided through filler needle 2209 to fill balloon 2202. For example, filler needle 2209 may be placed through shaft 2204 to balloon implant 2202 allowing deposition of bone cement. Filler needle 2209 may have laser markings on the outside to aid in determining the correct depth for injecting bone cement. The diameter of filler needle 2209 may be determined such that the outside diameter of filler needle 2209 may have a clearance in relation to the inside diameter of shaft 2204 to allow for the venting of air, but not viscous liquids. This may aid in allowing for balloon implant 2202 to void entirely of air while being filled with bone cement.
  • Hub 2206 is shown in greater detail in FIG. 28. Hub 2206 may lock onto an access cannula 2210, which may have a handle 2210. This configuration may prevent rotation or axial movement of the implantable device 2200. As shown in FIG. 28, wings 2214 of hub 2206 overlap handle 2210 and detents on hub 2206 may securely hold hub 2206 to handle 2210.
  • FIG. 23 illustrates balloon implant 2202 rigidly attached to shaft 2204. In this manner, a neck 2216 of balloon implant 2202 may be bonded to shaft 2204. Detachment of balloon implant 2202 from shaft 2204 is detailed with respect to FIGS. 26A-27.
  • FIGS. 26A and 26B illustrate a detachment device 2600, which may include jaws 2602. Detachment device 2600 may be a cannulated shaft, having multiple jaws 2602, that is inserted into shaft 2204 and extends to neck 2216. A mandrel may be inserted into the detachment device 2600 through its cannulation and force jaws 2602 to expand, as shown in FIG. 27.
  • FIG. 27 illustrates balloon implant 2202, neck 2216, cannula 2210, jaws 2602 of device 2600, and mandrel 2604. Upon insertion of mandrel 2604 through the cannulation of the detachment device 2600, jaws 2602 are forced to expand outwards towards the inner surface of cannula 2210, which interferes with the surface. Because of this, jaws 2602 cut through neck 2216 of balloon implant 2602 and detachment device 2600 is rotated to fully sever neck 2216 and allow it and balloon implant 2202 to remain in the vertebral body.
  • In another configuration, balloon implant 2202 may be releasably attached to shaft 2204. In FIG. 24, shaft 2204 may comprise two steel tubes 2218. Balloon implant 2202 may be disposed in a manner such that neck 2216 may be tightly sandwiched between steel tubes 2218. In order to release balloon implant 2202 from shaft 2204, one of steel tubes 2218 may be retracted thereby detaching balloon implant 2202 from shaft 2204.
  • FIG. 25 illustrates another manner in which balloon implant 2202 may be released from shaft 2204. Neck 2216 may be engaged with shaft 2204 through a threaded connection. In order to release balloon implant 2202 from shaft 2204, a user may rotate shaft 2204 until the threaded connection is undone thereby detaching balloon implant 2202 from shaft 2204.
  • FIG. 29 illustrates a method 2900 for delivering bone cement to a vertebral body consistent with the present disclosure. At step 2902, using access instrumentation and fluoroscopic guidance, a working cannula and introducer is used to access the desired vertebral body. At step 2904, after accessing the vertebral body, a scraper, curette, bone tamp, or any combination of the aforementioned may be used with fluoroscopic guidance to create a cavity within the cancellous bone of the vertebral body. The cavity size may correspond to the size of the balloon implant being used. The implant size may be designed to be larger than the cavity created such that the implant balloon does not stretch during cement filling. At step 2906, after selecting an appropriately sized implant, the user may insert the inflation device through the cannula. At step 2908, bone cement is first prepared by mixing the liquid and powder components. The cement may be injected though a filler needle. The filler delivery needle may be inserted through the shaft of the inflation device, into the balloon implant under fluoroscopic guidance. At step 2910, after the cement has cured within the balloon implant, the balloon implant may be separated through detachment, unthreading, or separation and left to remain within the vertebral body.
  • While it is apparent that the invention disclosed herein is well calculated to fulfill the objects stated above, it will be appreciated that numerous modifications and embodiments may be devised by those skilled in the art.

Claims (20)

What is claimed is:
1. A method for repairing a vertebral body, said method comprising:
accessing the vertebral body via a cannula;
creating a cavity within cancellous bone of the vertebral body;
inserting an implantable device into the cavity via the cannula, wherein the implantable device comprises:
a balloon implant having a neck portion and configured to receive bone cement, wherein the balloon implant has a larger size than the cavity;
a shaft rigidly attached to the neck portion at a distal end;
a hub attached to shaft at a proximal end; and
a filler needle disposed inside the shaft and configured to provide bone cement to the balloon implant;
delivering bone cement to the balloon implant;
detaching the balloon implant from the shaft via a detachment device, wherein the detachment device has two or more jaws configured to radially cut the balloon implant when rotated within the shaft.
2. The method of claim 1, wherein the balloon implant and the shaft are bonded together.
3. The method of claim 1, wherein the hub is configured to attach to a handle of the cannula.
4. The method of claim 3, wherein the hub is configured to prevent at least one of rotation and axial movement of the implantable device.
5. The method of claim 4, wherein the hub contains one or more wings to overlap the handle.
6. The method of claim 1, wherein the jaws of the detachment device are driven open by a mandrel inserted in a cannulated portion of the detachment device.
7. The method of claim 1, wherein the filler needle includes markings indicating a depth of the needle into the balloon implant.
8. The method of claim 1, wherein the filler needle is configured to provide a clearance between the filler needle and the shaft to provide venting for air while maintaining liquid within the balloon implant.
9. An implantable device for repairing a vertebral body, said implantable device comprising:
a balloon implant having a neck portion and configured to receive bone cement, wherein the balloon implant has a larger size than the cavity;
a shaft rigidly attached to the neck portion at a distal end;
a hub attached to shaft at a proximal end; and
a filler needle disposed inside the shaft and configured to provide bone cement to the balloon implant;
a detachment device having two or more jaws configured to radially cut the balloon implant when rotated within the shaft.
10. The device of claim 9, wherein the balloon implant and the shaft are bonded together.
11. The device of claim 9, wherein the hub is configured to attach to a handle of the cannula.
12. The device of claim 11, wherein the hub is configured to prevent at least one of rotation and axial movement of the implantable device.
13. The device of claim 12, wherein the hub contains one or more wings to overlap the handle.
14. The device of claim 9, wherein the jaws of the detachment device are driven open by a mandrel inserted in a cannulated portion of the detachment device.
15. The device of claim 9, wherein the filler needle includes marking indicating a depth of the needle into the balloon implant.
16. The device of claim 9, wherein the filler needle is configured to provide a clearance between the filler needle and the shaft to provide venting for air while maintaining liquid within the balloon implant.
17. An implantable device for repairing a vertebral body, said implantable device comprising:
a balloon implant having a neck portion and configured to receive bone cement, wherein the balloon implant has a larger size than the cavity;
a shaft attached to the neck portion at a distal end;
a hub attached to shaft at a proximal end; and
a filler needle disposed inside the shaft and configured to provide bone cement to the balloon implant.
18. The device of claim 17, wherein the shaft further comprises a pair of steel tubes and the neck portion is disposed between the steel tubes and wherein the balloon implant is released from the shaft by retracting one of the pair of steel tubes.
19. The device of claim 17, wherein the shaft is attached to the neck portion via threaded connection.
20. The device of claim 19, wherein the shaft is configured to rotate to release the balloon implant from the threaded connection.
US15/728,581 2009-12-07 2017-10-10 Methods and apparatus for treating vertebral fractures Abandoned US20180085150A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US15/728,581 US20180085150A1 (en) 2009-12-07 2017-10-10 Methods and apparatus for treating vertebral fractures
EP18199049.0A EP3470000A1 (en) 2017-10-10 2018-10-08 Apparatus for treating vertebral fractures
JP2018191439A JP2019069151A (en) 2009-12-07 2018-10-10 Methods and apparatus for treating vertebral fractures

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US12/632,325 US8734458B2 (en) 2009-12-07 2009-12-07 Methods and apparatus for treating vertebral fractures
US14/254,614 US9526550B2 (en) 2009-12-07 2014-04-16 Methods and apparatus for treating vertebral fractures
US15/355,100 US20170065309A1 (en) 2009-12-07 2016-11-18 Methods and apparatus for treating vertebral fractures
US15/728,581 US20180085150A1 (en) 2009-12-07 2017-10-10 Methods and apparatus for treating vertebral fractures

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US15/355,100 Continuation-In-Part US20170065309A1 (en) 2009-12-07 2016-11-18 Methods and apparatus for treating vertebral fractures

Publications (1)

Publication Number Publication Date
US20180085150A1 true US20180085150A1 (en) 2018-03-29

Family

ID=44082738

Family Applications (4)

Application Number Title Priority Date Filing Date
US12/632,325 Active 2031-02-08 US8734458B2 (en) 2009-12-07 2009-12-07 Methods and apparatus for treating vertebral fractures
US14/254,614 Active 2030-07-25 US9526550B2 (en) 2009-12-07 2014-04-16 Methods and apparatus for treating vertebral fractures
US15/355,100 Abandoned US20170065309A1 (en) 2009-12-07 2016-11-18 Methods and apparatus for treating vertebral fractures
US15/728,581 Abandoned US20180085150A1 (en) 2009-12-07 2017-10-10 Methods and apparatus for treating vertebral fractures

Family Applications Before (3)

Application Number Title Priority Date Filing Date
US12/632,325 Active 2031-02-08 US8734458B2 (en) 2009-12-07 2009-12-07 Methods and apparatus for treating vertebral fractures
US14/254,614 Active 2030-07-25 US9526550B2 (en) 2009-12-07 2014-04-16 Methods and apparatus for treating vertebral fractures
US15/355,100 Abandoned US20170065309A1 (en) 2009-12-07 2016-11-18 Methods and apparatus for treating vertebral fractures

Country Status (4)

Country Link
US (4) US8734458B2 (en)
EP (1) EP2509520B1 (en)
JP (2) JP5690841B2 (en)
WO (1) WO2011071851A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11337741B2 (en) 2020-05-01 2022-05-24 Sergio Lenchig Laterally deployed kyphoplasty balloon tamponade

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10154163A1 (en) * 2001-11-03 2003-05-22 Advanced Med Tech Device for straightening and stabilizing the spine
US7955339B2 (en) * 2005-05-24 2011-06-07 Kyphon Sarl Low-compliance expandable medical device
US7806900B2 (en) 2006-04-26 2010-10-05 Illuminoss Medical, Inc. Apparatus and methods for delivery of reinforcing materials to bone
US7879041B2 (en) 2006-11-10 2011-02-01 Illuminoss Medical, Inc. Systems and methods for internal bone fixation
JP5442444B2 (en) 2006-11-10 2014-03-12 イルミンオス・メディカル・インコーポレイテッド System and method for internal bone fixation
US9427289B2 (en) 2007-10-31 2016-08-30 Illuminoss Medical, Inc. Light source
US8403968B2 (en) 2007-12-26 2013-03-26 Illuminoss Medical, Inc. Apparatus and methods for repairing craniomaxillofacial bones using customized bone plates
AU2010328680B2 (en) 2009-08-19 2014-10-23 Illuminoss Medical, Inc. Devices and methods for bone alignment, stabilization and distraction
US8282628B2 (en) * 2009-10-26 2012-10-09 Globus Medical, Inc. Vertebral body nerve and vein cauterizing system and method
US11090092B2 (en) 2009-12-07 2021-08-17 Globus Medical Inc. Methods and apparatus for treating vertebral fractures
US9358058B2 (en) 2012-11-05 2016-06-07 Globus Medical, Inc. Methods and apparatus for treating vertebral fractures
US9326799B2 (en) * 2009-12-07 2016-05-03 Globus Medical, Inc. Methods and apparatus for treating vertebral fractures
US9220554B2 (en) 2010-02-18 2015-12-29 Globus Medical, Inc. Methods and apparatus for treating vertebral fractures
US8992540B2 (en) * 2010-07-22 2015-03-31 Kyphon Sarl Adjustable surgical instruments and methods of use and fabrication
EP2654584A1 (en) 2010-12-22 2013-10-30 Illuminoss Medical, Inc. Systems and methods for treating conditions and diseases of the spine
US8394129B2 (en) 2011-03-10 2013-03-12 Interventional Spine, Inc. Method and apparatus for minimally invasive insertion of intervertebral implants
US8518087B2 (en) 2011-03-10 2013-08-27 Interventional Spine, Inc. Method and apparatus for minimally invasive insertion of intervertebral implants
US9775661B2 (en) 2011-07-19 2017-10-03 Illuminoss Medical, Inc. Devices and methods for bone restructure and stabilization
ITRM20110479A1 (en) * 2011-09-09 2013-03-10 O P A Medical S R L GROUP FOR CIFOPLASTIC INTERVENTIONS
WO2013059609A1 (en) 2011-10-19 2013-04-25 Illuminoss Medical, Inc. Systems and methods for joint stabilization
WO2013082497A1 (en) * 2011-11-30 2013-06-06 Beth Israel Deaconess Medical Center Systems and methods for endoscopic vertebral fusion
US10034700B2 (en) * 2012-02-17 2018-07-31 DePuy Synthes Products, Inc. Adjustable balloon including bone access tip
JP5989488B2 (en) 2012-09-28 2016-09-07 テルモ株式会社 Spacers and expansion devices
US9687281B2 (en) 2012-12-20 2017-06-27 Illuminoss Medical, Inc. Distal tip for bone fixation devices
US9387030B2 (en) * 2013-01-07 2016-07-12 Kyphon SÀRL Catheter with integrated cement delivery balloon
US9192420B2 (en) 2013-01-24 2015-11-24 Kyphon Sarl Surgical system and methods of use
US9351779B2 (en) * 2013-01-25 2016-05-31 Kyphon SÀRL Expandable device and methods of use
US9277928B2 (en) 2013-03-11 2016-03-08 Interventional Spine, Inc. Method and apparatus for minimally invasive insertion of intervertebral implants
US9993353B2 (en) 2013-03-14 2018-06-12 DePuy Synthes Products, Inc. Method and apparatus for minimally invasive insertion of intervertebral implants
US20140378980A1 (en) * 2013-06-24 2014-12-25 Roman Lomeli Cortical Rim-Supporting Interbody Device
US10806593B2 (en) * 2013-06-24 2020-10-20 DePuy Synthes Products, Inc. Cortical rim-supporting interbody device
WO2015120155A1 (en) * 2014-02-06 2015-08-13 Boston Scientific Scimed, Inc. Occlusion device detachable by inflation of a balloon
US11154302B2 (en) 2014-03-31 2021-10-26 DePuy Synthes Products, Inc. Aneurysm occlusion device
US11076860B2 (en) 2014-03-31 2021-08-03 DePuy Synthes Products, Inc. Aneurysm occlusion device
US10231770B2 (en) 2015-01-09 2019-03-19 Medtronic Holding Company Sárl Tumor ablation system
US20160354130A1 (en) * 2015-06-02 2016-12-08 Kyphon SÀRL Bone tamp and method of use
CN105343992A (en) * 2015-09-29 2016-02-24 上海凯利泰医疗科技股份有限公司 Adjustable high-pressure-expansion balloon bag
KR20190115474A (en) 2017-02-23 2019-10-11 디퍼이 신테스 프로덕츠, 인코포레이티드 Aneurysm device and delivery system
US10905430B2 (en) 2018-01-24 2021-02-02 DePuy Synthes Products, Inc. Aneurysm device and delivery system
US11596412B2 (en) 2018-05-25 2023-03-07 DePuy Synthes Products, Inc. Aneurysm device and delivery system
US11058430B2 (en) * 2018-05-25 2021-07-13 DePuy Synthes Products, Inc. Aneurysm device and delivery system
US10939915B2 (en) 2018-05-31 2021-03-09 DePuy Synthes Products, Inc. Aneurysm device and delivery system
WO2020006239A1 (en) 2018-06-27 2020-01-02 Illuminoss Medical, Inc. Systems and methods for bone stabilization and fixation
US11051825B2 (en) 2018-08-08 2021-07-06 DePuy Synthes Products, Inc. Delivery system for embolic braid
US11123077B2 (en) 2018-09-25 2021-09-21 DePuy Synthes Products, Inc. Intrasaccular device positioning and deployment system
US11076861B2 (en) * 2018-10-12 2021-08-03 DePuy Synthes Products, Inc. Folded aneurysm treatment device and delivery method
US11406392B2 (en) 2018-12-12 2022-08-09 DePuy Synthes Products, Inc. Aneurysm occluding device for use with coagulating agents
US11272939B2 (en) 2018-12-18 2022-03-15 DePuy Synthes Products, Inc. Intrasaccular flow diverter for treating cerebral aneurysms
US11134953B2 (en) 2019-02-06 2021-10-05 DePuy Synthes Products, Inc. Adhesive cover occluding device for aneurysm treatment
US11337706B2 (en) 2019-03-27 2022-05-24 DePuy Synthes Products, Inc. Aneurysm treatment device
CN110236744B (en) * 2019-04-24 2021-07-30 宁波华科润生物科技有限公司 Minimally invasive fusion cage
US11602350B2 (en) 2019-12-05 2023-03-14 DePuy Synthes Products, Inc. Intrasaccular inverting braid with highly flexible fill material
US11497504B2 (en) 2019-05-21 2022-11-15 DePuy Synthes Products, Inc. Aneurysm treatment with pushable implanted braid
US11278292B2 (en) 2019-05-21 2022-03-22 DePuy Synthes Products, Inc. Inverting braided aneurysm treatment system and method
US10653425B1 (en) 2019-05-21 2020-05-19 DePuy Synthes Products, Inc. Layered braided aneurysm treatment device
US11607226B2 (en) 2019-05-21 2023-03-21 DePuy Synthes Products, Inc. Layered braided aneurysm treatment device with corrugations
US11413046B2 (en) 2019-05-21 2022-08-16 DePuy Synthes Products, Inc. Layered braided aneurysm treatment device
US11672542B2 (en) 2019-05-21 2023-06-13 DePuy Synthes Products, Inc. Aneurysm treatment with pushable ball segment
US11457926B2 (en) 2019-12-18 2022-10-04 DePuy Synthes Products, Inc. Implant having an intrasaccular section and intravascular section
US11484355B2 (en) * 2020-03-02 2022-11-01 Medtronic Holding Company Sàrl Inflatable bone tamp and method for use of inflatable bone tamp
US11376131B2 (en) * 2020-04-07 2022-07-05 Ethicon, Inc. Cortical rim-supporting interbody device and method
US11298238B1 (en) * 2021-07-23 2022-04-12 Focus Medical Company, Llc Balloon kyphoplasty surgical device and method

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100076503A1 (en) * 2007-02-07 2010-03-25 N.M.B. Medical Applications Ltd Bone implant

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4969888A (en) * 1989-02-09 1990-11-13 Arie Scholten Surgical protocol for fixation of osteoporotic bone using inflatable device
CA2007210C (en) * 1989-05-10 1996-07-09 Stephen D. Kuslich Intervertebral reamer
US6248110B1 (en) * 1994-01-26 2001-06-19 Kyphon, Inc. Systems and methods for treating fractured or diseased bone using expandable bodies
US5571189A (en) * 1994-05-20 1996-11-05 Kuslich; Stephen D. Expandable fabric implant for stabilizing the spinal motion segment
US20050131269A1 (en) * 1995-06-07 2005-06-16 Talmadge Karen D. System and method for delivering a therapeutic agent for bone disease
CA2683004A1 (en) * 1995-06-07 1996-12-19 Kyphon Sarl Expandable devices for treatment of fractured or diseased bone
FR2742994B1 (en) * 1995-12-28 1998-04-03 Sgro Jean-Claude INTRACORPOREAL LIGHT SURGICAL TREATMENT ASSEMBLY
KR100480402B1 (en) * 1996-11-26 2005-04-06 에드워즈 라이프사이언시스 코포레이션 Multiple lumen access device
AU8386798A (en) 1997-07-09 1999-02-08 Tegementa, L.L.C. Interbody device and method for treatment of osteoporotic vertebral collapse
US6440138B1 (en) * 1998-04-06 2002-08-27 Kyphon Inc. Structures and methods for creating cavities in interior body regions
NZ508401A (en) * 1998-06-01 2003-07-25 Kyphon Inc Expandable preformed structures for deployment in interior body regions
ATE318559T1 (en) * 2000-04-05 2006-03-15 Kyphon Inc DEVICES FOR TREATING BROKEN AND/OR DISEASE BONES
US6964667B2 (en) * 2000-06-23 2005-11-15 Sdgi Holdings, Inc. Formed in place fixation system with thermal acceleration
US20020068974A1 (en) * 2000-07-21 2002-06-06 Kuslich Stephen D. Expandable porous mesh bag device and methods of use for reduction, filling, fixation and supporting of bone
US6632235B2 (en) * 2001-04-19 2003-10-14 Synthes (U.S.A.) Inflatable device and method for reducing fractures in bone and in treating the spine
US20050209629A1 (en) * 2001-04-19 2005-09-22 Kerr Sean H Resorbable containment device and process for making and using same
US6746451B2 (en) * 2001-06-01 2004-06-08 Lance M. Middleton Tissue cavitation device and method
DE10154163A1 (en) * 2001-11-03 2003-05-22 Advanced Med Tech Device for straightening and stabilizing the spine
DE602004018903D1 (en) * 2003-02-14 2009-02-26 Depuy Spine Inc IN-SITU MANUFACTURED INTERVERTEBRALE FUSION DEVICE
TW587932B (en) * 2003-05-21 2004-05-21 Guan-Gu Lin Removable animal tissue filling device
US20050015150A1 (en) * 2003-07-17 2005-01-20 Lee Casey K. Intervertebral disk and nucleus prosthesis
US20060100706A1 (en) * 2004-11-10 2006-05-11 Shadduck John H Stent systems and methods for spine treatment
PE20060861A1 (en) * 2005-01-07 2006-10-25 Celonova Biosciences Inc IMPLANTABLE THREE-DIMENSIONAL BONE SUPPORT
JP2006263184A (en) * 2005-03-24 2006-10-05 Gc Corp Bone cement injection and filling method and leakage prevention bag for injecting and filling bone cement
EP1909671B1 (en) * 2005-07-11 2012-01-18 Kyphon SÀRL System for inserting biocompatible filler materials in interior body regions
ITMI20060502A1 (en) * 2006-03-21 2007-09-22 Maus Italia F Agostino & C Sas MULTI-PURPOSE EXPANSION WORKING DEVICE FOR CUTTING OR EXPANSION OF METAL TUBES
US20070276491A1 (en) * 2006-05-24 2007-11-29 Disc Dynamics, Inc. Mold assembly for intervertebral prosthesis
WO2008109695A2 (en) * 2007-03-06 2008-09-12 Orthobond, Inc. Preparation tools and methods of using the same
US20080249604A1 (en) * 2007-03-30 2008-10-09 Brian Donovan Apparatus and method for medical procedures within a spine
WO2009064847A2 (en) * 2007-11-16 2009-05-22 Synthes (U.S.A.) Porous containment device and associated method for stabilization of vertebral compression fractures
JP2009142563A (en) * 2007-12-17 2009-07-02 Olympus Terumo Biomaterials Corp Balloon and centrum setting tool
WO2009084109A1 (en) * 2007-12-28 2009-07-09 Olympus Terumo Biomaterials Corp. Unit for resetting bone fracture caused by pyramidal compression
US8292961B2 (en) * 2008-01-23 2012-10-23 Osman Said G Biologic vertebral reconstruction
JP2008173498A (en) * 2008-03-07 2008-07-31 Kenji Yoshida Card with dot pattern
US9186488B2 (en) * 2008-06-02 2015-11-17 Loma Vista Medical, Inc. Method of making inflatable medical devices
WO2009152470A1 (en) * 2008-06-13 2009-12-17 The Foundry, Llc. Methods and apparatus for joint distraction
US9358058B2 (en) * 2012-11-05 2016-06-07 Globus Medical, Inc. Methods and apparatus for treating vertebral fractures
JP2011125979A (en) * 2009-12-18 2011-06-30 Hotoku Kikai Kogyo Kk Pipe cutter
WO2011075672A1 (en) * 2009-12-18 2011-06-23 Hollowell Dan R Apparatus and methods for detaching an expandable member from a medical device
US20130072941A1 (en) * 2011-09-16 2013-03-21 Francisca Tan-Malecki Cement Injector and Cement Injector Connectors, and Bone Cement Injector Assembly

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100076503A1 (en) * 2007-02-07 2010-03-25 N.M.B. Medical Applications Ltd Bone implant

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11337741B2 (en) 2020-05-01 2022-05-24 Sergio Lenchig Laterally deployed kyphoplasty balloon tamponade

Also Published As

Publication number Publication date
WO2011071851A1 (en) 2011-06-16
US20170065309A1 (en) 2017-03-09
EP2509520B1 (en) 2019-04-03
EP2509520A1 (en) 2012-10-17
JP2013512761A (en) 2013-04-18
EP2509520A4 (en) 2014-10-29
US20140303633A1 (en) 2014-10-09
JP2019069151A (en) 2019-05-09
JP5690841B2 (en) 2015-03-25
US8734458B2 (en) 2014-05-27
US9526550B2 (en) 2016-12-27
US20110137317A1 (en) 2011-06-09

Similar Documents

Publication Publication Date Title
US20180085150A1 (en) Methods and apparatus for treating vertebral fractures
US9220554B2 (en) Methods and apparatus for treating vertebral fractures
US8226717B2 (en) Methods and devices for treating fractured and/or diseased bone using an expandable stent structure
US9554840B2 (en) Low cost low profile inflatable bone tamp
US20030050644A1 (en) Systems and methods for accessing and treating diseased or fractured bone employing a guide wire
WO2005048856A1 (en) Expandable implant for treating fractured and/or collapsed bone
EP3470000A1 (en) Apparatus for treating vertebral fractures
US10517660B2 (en) Multichannel cannula for kyphoplasty and method of use
WO2013074933A1 (en) Systems and methods for minimally invasive fracture reduction and fixation
WO2023076529A1 (en) System and device for performing vertebral augmentation

Legal Events

Date Code Title Description
AS Assignment

Owner name: GLOBUS MEDICAL, INC., PENNSYLVANIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:O'HALLORAN, DAMIEN;PAUL, DAVID C.;SUH, SEAN;AND OTHERS;SIGNING DATES FROM 20081001 TO 20171110;REEL/FRAME:044129/0548

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION