Abstract: A prosthetic device and method of inserting same between adjacent vertebrae, according to which a first member of a relatively flexible material is adapted to extend between the vertebrae; and at least one second member of a relatively stiff material is supported by the first member.

Abstract: An intervertebral prosthetic device and method for spinal stabilization, according to which a prosthetic device is implanted relative to two vertebrae and is positioned so that it makes a rigid connection with one of the vertebra and a non-rigid connection with the other vertebra.

Abstract: A prosthetic device and a method of implanting same between two vertebrae of a vertebral column to stabilize the column, according to which each vertebrae is engaged by a spacer, and the spacers are connected to permit relative movement between the spacers so that the distance between the spacers can vary to conform with the distance between the vertebrae and accommodate bending movements of the vertebral column.

Abstract: A composite spinal implant device including collagen and/or synthetic fibers impregnated with a bioactive formulation is disclosed. Also disclosed are methods of making the composite spinal implant devices, surgeries using the device, and kits containing the device.

Abstract: The forces exerted on a spinal implant by one or more coupling assemblies are controlled to facilitate the use of the implant in spinal stabilization and other procedures. The coupling assemblies are structured to distribute the forces exerted on the implant while engaging the implant to the coupling assembly and providing at least one of a rigid, semi-rigid or variable engagement of the coupling assembly with one or more anatomical structures of the spinal column.

Abstract: One embodiment of the present application includes: performing a medical procedure on a segment of a patient's spine. This segment includes two vertebrae each in contact with a spinal disk positioned in an intervertebral disk space. A passage is formed that follows a pathway through the vertebrae and the intervertebral disk space. This passage extends from an extradiscal opening through one of the vertebrae along a path that turns to change direction. The tubular device is inserted in the passage and extends through the intervertebral disk space. A fluid material is introduced into the tubular device to at least partially fill it to provide a spinal prosthetic structure. Other embodiments and inventive aspects include other prosthetic device arrangements, implantation methods, systems, and techniques.

Abstract: The invention provides a fixation device for implantation in a patient to provide support to a body component. The fixation device includes an outer construct forming a pocket and a slurry disposed in the pocket. The slurry is comprised of magnetic particles. The slurry is responsive to an electric field to modulate stiffness of the slurry. A system is provided to generate the electric field. Further, a method is provided to use the fixation device.

Abstract: Systems and methods for multi-directional stabilization of a spinal column segment are provided. The systems include one or more motion preserving constructs that are engaged to adjacent vertebrae and extend trans-axially between the vertebrae obliquely to the central axis of the spinal column. The systems permit motion of at least a portion of a vertebral level while providing stabilization at least when tensioned. Systems that provide stabilization in compression are also contemplated.

Abstract: A prosthetic device and a method for inserting same between adjacent vertebrae, according to which two connected members are provided, one of which is formed by a relatively flexible material and the other of which is formed by a relatively stiff material.

Abstract: Systems and methods for multi-level, multi-functional stabilization of a spinal column segment are provided. The systems include one or more constructs having a motion preserving portion that permits motion of at least a portion of a vertebral level and a motion preventing portion that substantially prevents motion of at least a portion of a second, adjacent vertebral level.

Abstract: Intervertebral implant components having compliant coatings, and methods of making and implanting the implant components are provided. The embodiments relate to compositions, methods and devices having a compliant surface coating that permits application of the device in areas without significant bone reformation to accept the device.

Abstract: An instrument for tensioning a flexible elongate member in a surgical procedure includes a tensioning mechanism engageable to a portion of the flexible elongate member and operable to apply a tensioning force to the elongate member. The instrument includes a distal end portion at a distal end of the tensioning mechanism that is adapted to allow orientation of the elongate member in a first direction for implantation and to allow the instrument to extend transversely to the implantation orientation during application of a tensioning force. The distal end portion can also include a receptacle to receive a structure at the surgical site to facilitate positioning of the distal end portion at the desired location.

Abstract: A posterior spinal fixation device or dynamic spinal stabilization device or other orthopedic device includes an active agent-delivery component. The active agent-delivery component has an active agent impregnated therein or adsorbed thereon or otherwise contained therein and is configured to release the active agent locally after the device is implanted in a patient. One preferred type of implant in accordance with the invention is an implant for stabilizing a spinal motion segment that includes a spacer member positionable between adjacent spinous processes or transverse processes or other posterior spinal element, including an implanted anchor element.

Abstract: Embodiments include a method for promoting selective tissue attachment to medical implants. By treating implant surfaces where tissue attachment is desired with tissue attachment promoting treatments, and treating implant surfaces where tissue attachment is not desired with tissue attachment inhibiting treatments, selective tissue attachment to medical implants may be achieved. Also, embodiments include an implant with at least one tissue contacting surface and at least one secondary surface where tissue attachment is not desired, and appropriate tissue attachment promoting or inhibiting treatments on the surfaces.

Abstract: A method of making a component of a spinal fixation system. The method may comprise providing a mixture of a powder of at least one metal or metal alloy and a polymeric binder. A metal-injection-molding process may use the mixture to form a component for a spinal fixation system. The components may have varying flexibility across their cross-sections. Also, components are provided that are produced by this process, such as spinal fixation rods and plates.

Abstract: Embodiments provide composite components for use in spinal fixation systems. The composite components may comprise polyetheretherketone (PEEK) or another non-resorbable or resorbable polymeric material and at least one metal. Incorporation of PEEK or another non-resorbable or resorbable polymeric material into the components allows average or mean physical properties (e.g., tensile strength, modulus of elasticity, etc.) of the components to be modulated. The composition and orientation of the composite components can be advantageously chosen to produce components with desired physical characteristics.

Abstract: One technique of the present application includes: evaluating a patient having a previously implanted spinal construct and corresponding spinal fusion from an earlier procedure and determining a spinal segment adjacent to the spinal fusion is degenerating after completion of the earlier procedure. After this determination, the previously implanted spinal construct is augmented by attaching a flexible polymer elongated member to the spinal segment adjacent to the spinal fusion with a bone fastener and by coupling the flexible polymer elongated member to one or more elements of the previously implanted spinal construct. In one form, the elongated member is at least partially comprised of polyetheretherketone.

Abstract: At least a portion of an articulating surface of a facet arthroplasty device may comprise a polycrystalline diamond compact. The polycrystalline diamond compact may be useful to increase the wearability and decrease the coefficient of friction of the at least one articulating surface of the facet arthroplasty device. The polycrystalline diamond compact may be utilized with any facet arthroplasty device and may be formed by any appropriate method including, but not limited to, diamond sintering, chemical vapor deposition, physical vapor deposition, and energy beam ablation/deposition.

Abstract: One embodiment of the present application includes a spinal disk prosthesis with one end portion to form a load transmitting relationship with one vertebra of a patient's spine and another end portion to form a load transmitting relationship with another vertebra of the patient's spine. A tube connects the end portions together and a damping material is positioned inside the tube. The end portions each include a magnet to generate a corresponding magnetic field. These magnetic fields are oriented to provide a repulsive force between the end portions to provide a magnetic bearing.

Abstract: Embodiments include coatings or surface treatments for medical instruments, devices, and/or implants that promote soft tissue healing. More particularly, embodiments relate to treating portions of instruments, devices, and implants where tissue healing is desired with tissue healing promoting treatments.