Abstract: A device and method for stabilizing a spine utilizes one or more stabilization members made of, or including, a bioresorbable and/or biointegrable material such as natural tissue or a bioresorbable polymer. The stabilization member(s) may be elastic, and may secure one or more spinal motion segments in a manner effective to reduce the range of flexion and/or extension of the spinal motion segments. The stabilization member may include one or more elongate straps of nonosteogenic natural tissue, each of which may be secured to the spine using fasteners such as bone screws or tacks. The stabilization device may include a blocking member sized and configured to be effective for maintaining a medically desirable distance between adjacent spinous processes in the spine of a medical patient.

Abstract: A nucleus implant is disclosed. The nucleus implant can be configured to be installed within an intervertebral disc between an inferior vertebra and a superior vertebra. The nucleus implant can include an expandable core and an expandable chamber that can be disposed at least partially around the expandable core. The expandable chamber can be expanded from a deflated position to an inflated position. Further, a hardness of the expandable core when inflated can greater than or equal to a hardness of the expandable chamber when inflated.

Abstract: A targeting surgical instrument for use in spinal disc replacement includes a first arm, a second arm and a body portion. The first arm is configured to be longitudinally aligned with a mid-line of a spine and to be at least partially received on an endplate of a lower vertebra of spinal cavity. The spinal cavity is defined by a lower vertebra and an upper vertebra of the spinal cavity. The second arm is positioned at an angle relative to the first arm. The second arm defines an insertion angle for a spinal implant. The body portion connects the first arm and the second arm. The body portion includes a plurality of radial opaque markers located to allow alignment of the first arm on the mid-line of the spine.

Abstract: A nucleus implant is disclosed. The nucleus implant can be configured to be installed within an intervertebral disc between an inferior vertebra and a superior vertebra. Further, the nucleus implant can include a solid core and an expandable chamber that can be disposed at least partially around the solid core. The expandable chamber can be expanded from a deflated position to an inflated position.

Abstract: An instrument for separating adjacent vertebrae includes a handle assembly and a distal portion at a distal end of the handle assembly. The distal portion includes first and second members movable from an unexpanded configuration for insertion in the disc space toward an expanded configuration to separate the vertebrae. A cutting member of a cutting instrument can be guided by the instrument to prepare the vertebrae for engagement with an implant.

Abstract: A system for forming a spinal prosthesis in situ within an intervertebral space located between first and second adjacent vertebrae includes at least one mold having at least one internal compartment adapted to receive at least one flowable biomaterial. The system also includes a retaining member adapted to secure the mold between the first and second vertebrae, the retaining member including first and second portions adapted to be engaged with first and second surfaces of the first and second vertebrae, respectively. The retaining member also includes an intermediate body operatively coupling the first portion to the second portion, the intermediate body adapted to be positioned in or adjacent to the intervertebral space. A biomaterial delivery apparatus is in fluid communication with the mold at a pressure sufficient for the mold to engage with the retaining member. The spinal prosthesis selectively position the first vertebrae relative to the second vertebrae.

Abstract: A nuclectomy method for creating a nuclear cavity in an annulus located in an intervertebral disc space and for preparing the nuclear cavity to receive an intervertebral prosthesis. The method involves identifying a plurality of regions in at least a portion of the nucleus. A sequence for removing the regions is also determined. At least one annulotomy is formed in the annulus along an annular axis to provide access to the nucleus. A guide system is positioned relative to the annulotomy. The guide system is configured to limit motion of at least one surgical tool relative to the guide system. A portion of the nucleus is removed from a first region using the surgical tool. At least one of the guide system and the surgical tool are configured to remove a portion of the nucleus from a second region. A portion of the nucleus is removed from a second region using the surgical tool.

Abstract: A method of stabilizing adjacent vertebrae including the steps of forming at least one annulotomy in an annulus. At least a portion of the nucleus material is removed through the annulotomy to form a cavity in an intervertebral disc space between the adjacent vertebrae. A reservoir containing a flowable biomaterial is fluidly coupled to the intervertebral disc space. A flowable biomaterial is delivered to the cavity. The delivery of the flowable biomaterial into the intervertebral disc space is controlled in accordance with at least a first operating parameter. The biomaterial is at least partially cured to stabilize the adjacent vertebrae.

Abstract: A prosthetic device for anterior-oblique insertion into an intervertebral space is provided. The prosthetic device includes a first component having a first flange for engaging a first vertebra from an anterior-oblique approach, the first flange being angled relative to the longitudinal and transverse axes of the first component, and a second component having a second flange for engaging a second vertebra from an anterior-oblique approach, the second flange being angled relative to the longitudinal and transverse axes of the second component, and wherein the first and second components cooperate to permit articulating motion between the first and second components.

Abstract: A method of implanting an intervertebral prosthesis in an intervertebral space between a first and a second vertebra of a patient's spinal column may include making a first aperture at a first location to permit access to the intervertebral disc space. The first aperture may be sized to allow passage of at least a portion of the intervertebral prosthesis. A second aperture may be made at a second location to permit access to the intervertebral disc space. The second aperture may be sized to allow passage of a surgical instrument. An intervertebral prosthesis for implantation into an intervertebral space between a first and a second vertebra of a patient's spinal column is also disclosed, along with a surgical instrument for implanting the an intervertebral prosthesis.

Abstract: The present application is directed to devices and methods for attaching one or more elongated members to a posterior surface of a vertebral member. The devices may include a body with a first face that contacts the vertebral member and a second opposite face. A hook may extend outward from the first face to engage the vertebral member. The body may also include one or more receivers to receive the elongated members. An engagement member may be movably connected to the body. The engagement member may include a first section that contacts the body, and a second section that includes a second hook. The engagement member may be positioned relative to the body to adjust a distance between the first and second hooks to attach the body to the vertebral member. A fastener may secure the engagement member to the body at the desired position. The fastener may also attach the one or more elongated members to the body.

Abstract: A prosthetic device for transforaminal insertion into an intervertebral space is provided. The prosthetic device includes a first component having a first curved flange for engaging a first vertebra from a transforaminal approach, the first component having a first articular surface, and a second component having a second curved flange for engaging a second vertebra from a transforaminal approach, the second component having a second articular surface for cooperating with the first articular surface to permit articulating motion between the first and second components.

Abstract: One embodiment is directed to instrumentation for performance of a spinal implantation procedure. In one form, this instrumentation includes: a tube device with an inner surface defining a passage from a proximal end portion to a distal end portion, a conveyor including a threaded conveying rod to be received in the passage of the tube device that can be rotated in the tube or moved in translation along the passage, and a deformable prosthesis structured to move through the passage of the tube by rotating the threaded conveying rod while at least a portion of the deformable prosthesis is positioned between the inner surface and the rod. Optionally, a tool to maintain position of the tube device can be included that has a jaw mechanism, among other things.

Abstract: A catheter holder designed to deliver a curable biomaterial to an intervertebral disc space. By securing the catheter to the catheter holder, the depth of insertion of the catheter into the disc space can be accurately controlled. The catheter holder optionally helps with insertion of a optional mold through the annulotomy and into the disc space created by the nuclectomy. The catheter holder helps keep the mold from being drawn too far into the disc space or pushed too far out of the disc space during polymer injection.

Abstract: A method of implanting an intervertebral prosthesis in a disc located between a pair of adjacent vertebrae of a patient. Damaged or diseased nucleus pulpous is removed from the disc using minimally invasive techniques. The adjacent vertebrae are positioned in a lordotic condition. A mold adapted to contain a biomaterial is positioned between the adjacent vertebrae. A flowable biomaterial is delivered into the mold using minimally invasive techniques so that the adjacent vertebrae are in the lordotic condition. The flowable biomaterial is allowed to at least partially cure so that the adjacent vertebrae are in a lordotic-neutral position.

Abstract: A plating system for stabilizing at least one level of the spinal column includes a plate member having a first portion with a bottom surface extending between opposite sides of the plate member. The bottom surface is positionable extradiscally along first and second vertebrae for engagement of the plate member thereto. A second portion of the plate member extends from one side of the first portion and away from the second side of the first portion. The second portion is received in the disc space between the first and second vertebrae and intradiscally engageable to at least one of the first and second vertebra.

Abstract: An intervertebral implant has two-plates intended to come into contact with a patient's vertebral end-plates. One of the plates has a cut-out delineating webs converging toward a zone where the plates are connected to one another.

Abstract: A plating system for stabilization of a bony segment includes a plate engageable to at least first and second bony elements. For spinal stabilization, the plate is attached at least to first and second vertebrae with at least one bone fastener in each vertebra. Retaining members are attachable to the plate to prevent the bone fasteners from backing out of the plate. One retaining member is a variable retaining member that allows the bone fasteners to toggle in the plate without interference. A second retaining member is a fixed retaining member that fixes the bone fasteners relative to the plate.

Abstract: A plating system for stabilization of a bony segment includes a plate engageable to at least first and second bony elements. For spinal stabilization, the plate is attached at least to first and second vertebrae with at least one bone fastener in each vertebra. Retaining members are attachable to the plate to prevent the bone fasteners from backing out of the plate. One retaining member is a variable retaining member that allows the bone fasteners to toggle in the plate without interference. A second retaining member is a fixed retaining member that fixes the bone fasteners relative to the plate.

Abstract: A method and apparatus for fluidly coupling a reservoir containing a flowable biomaterial to a mold. The flow of the flowable biomaterial into the mold is controlled in accordance with a first operating parameter. At least one injection condition is monitored. The flow of the flowable biomaterial is controlled in accordance with a second operating parameter in response to one or more of the injection conditions reaching a threshold level. The second operating parameter is maintained during at least a portion of the curing of the flowable biomaterial. In some embodiments, the second operating parameter may optionally include permitting a portion of the flowable biomaterial to be expelled from the mold.