A spinal disc implant including a body defined by a plurality of interwoven or braided nitinol strands. The body includes a first end and a second end. The nitinol strands come together at the first end and are secured with a first fitting. The nitinol strands also come together at the second end and are secured with a second fitting. The second fitting can include a snare hook. The braided nitinol skeleton is internally assembled within the intervertebral disc. The implant is filled with liquid, gel or silicone when utilized as a motion preserving nucleus pulpous implant. The implant is filled with bone graft material when utilized as an inter-body fusion implant. An instrument and technique that provides a minimally invasive needle based solution to address degenerative disc disease with enhanced structural integrity of the spine compared to conventional surgical devices and techniques.

Disclosed are devices, systems and/or methods for use in the surgical treatment of vertebrae and/or other bones, particularly implants and/or related devices comprising silicon nitride in some of all of the implant or device body, including portions, layers and/or surface coatings thereof, for use in spinal surgeries and/or other orthopedic procedures.

The present invention relates to methods of making a prosthesis or a stent with a smooth covering. The method includes providing an elastomeric tube including an inner diameter and an outer diameter, positioning the elastomeric tube in a tube expander including a vacuum, expanding the inner diameter and the outer diameters of the elastomeric tube by applying the vacuum, providing a mandrel, positioning an inner covering over the mandrel, positioning a stent over the inner covering, positioning an outer covering over the stent to form a covered stent, positioning the mandrel and the covered stent in the tube expander, releasing the vacuum, removing the elastomeric tube, the covered stent, and the mandrel form the tube expander, applying pressure and heat to the elastomeric tube, the covered stent, and the mandrel, removing the elastomeric tube, the covered stent, and the mandrel from the pressure and the heat, removing the elastomeric tube from the covered stent, and removing the mandrel from the covered stent.

The present invention relates to a stabilized ankle prosthesis configured for use in patients with compromised soft tissue in the ankle. The prosthesis of the present invention is a two-component design comprising a stabilizing lip configured to constrain movement in the general direction of compromised soft tissue.

Disclosed herein is an implant for use in a body, at least one portion of the surface of the implant being mutually engageable with at least one portion of at least one body part.

Also disclosed is a method of surgery comprising the steps of: forming an implant comprising at least one portion of the surface of the implant being mutually engageable with at least one portion of at least one body part, applying a layer of adhesive to the at least one portion of the surface, and engaging the at least one portion of the surface with the at least one portion of at least one body part.

The process for producing an orthopedic implant having an integrated silicon nitride surface layer includes steps for positioning the orthopedic implant inside a vacuum chamber, mixing nitrogen gas and vaporized silicon atoms in the vacuum chamber, emitting a relatively high energy beam into the mixture of nitrogen gas and vaporized silicon atoms in the vacuum chamber to cause a gas-phase reaction between the nitrogen gas and the vaporized silicon atoms to form reacted precipitate silicon nitride molecules, and driving the precipitate silicon nitride molecules with the same beam into an outer surface of the orthopedic implant at a relatively high energy such that the precipitate silicon nitride molecules implant therein and form at least a part of the molecular structure of the outer surface of the orthopedic implant, thereby forming the integrated silicon nitride surface layer.

A spinal disc implant including a body defined by a plurality of interwoven or braided nitinol strands. The body includes a first end and a second end. The nitinol strands come together at the first end and are secured with a first fitting. The nitinol strands also come together at the second end and are secured with a second fitting. The second fitting can include a snare hook. The braided nitinol skeleton is internally assembled within the intervertebral disc. The implant is filled with liquid, gel or silicone when utilized as a motion preserving nucleus pulpous implant. The implant is filled with bone graft material when utilized as an inter-body fusion implant. An instrument and technique that provides a minimally invasive needle based solution to address degenerative disc disease with enhanced structural integrity of the spine compared to conventional surgical devices and techniques.

Disclosed are devices, systems and/or methods for use in the surgical treatment of vertebrae and/or other bones, particularly implants and/or related devices comprising silicon nitride in some of all of the implant or device body, including portions, layers and/or surface coatings thereof, for use in spinal surgeries and/or other orthopedic procedures.

Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.

Disclosed is a spinal complex cage, which includes a cage which is made of a polymeric material, and metal covers which are formed on upper and lower portions of the cage, respectively, in which couplers formed on the metal covers are coupled to coupling grooves formed in the cage, such that the metal covers are detachably coupled to the upper and lower portions of the cage. Accordingly, because the cage and the metal cover are detachably coupled to each other, the manufacturing method is simple, and the metal cover is easily coupled to or separated from the cage, such that the spinal complex cage may be variously and quickly applied even during the surgery in accordance with shapes or intervals between the vertebral bodies, and as a result, a spinal fusion rate is excellent, and the accurate and precise surgical operation is enabled.