A glenoid implant for a shoulder prosthesis for implantation in the glenoid of a scapula according to embodiments of the present invention includes a central fixation element; an articular body configured for articulation with a humerus, the articular body comprising a plate, the plate comprising a side configured to be oriented toward the glenoid, the side comprising a central protrusion, wherein the central fixation element comprises a means for mechanically engaging with the central protrusion; a first means for locking rotation of the central fixation element with respect to the glenoid; and a second means for locking rotation of the articular body with respect to the glenoid.

An outer shell (1) for a joint socket implant, in particular for an acetabular implant, which comprises a convex outer face (3) and a concave inner face (4) for receiving an inner shell. The concave inner face (4) has at least partially a toothing system (7), in particular a circular circumferential region (6) thereof. Via the toothing system (7), an inhibition of the rotatability of the two shells, relative to one another, can be achieved upon insertion of the inner shell into the outer shell (1).

The glenoid implant comprises a baseplate, an articular component which has a convex articular surface, and a platform which is provided both to be secured to the articular component by a first attachment and to be secured to the baseplate by a second attachment, the first attachment being independent from the second attachment and defining an assembly axis along which the platform and the articular component are assembled together. The first attachment comprises both a translational connection that is intraoperatively operable to prevent translation between the platform and the articular component along the assembly axis, and a rotational connection that is intraoperatively operable to prevent rotation between the platform and the articular component around the assembly axis, the translational connection and the rotational connection being distinct from each other. The glenoid implant allows assembling the platform indifferently with one of various articular components which differ from each other for example by their material composition and/or by some geometric features of their convex articular surface and/or etc. The articular component that is effectively assembled with the platform can be chosen by the surgeon during surgery, i.e. during an implantation operation or just before the latter.

A geared cam expandable spinal implant. Rotational motion of a rotating portion is translated into linear motion of a yoke, which moves geared cams at the distal end of the implant to mate with, and walk along, teeth of corresponding racks. The walking of the gear cam teeth along the rack teeth creates a regular rate of implant expansion, reduces initial excessive expansion force applied to the implant, and provides fine adjustment of the expansion rate and force.

An expandable spinal interbody implant is provided that includes first/second components that are movable between collapsed and expanded states. Spaced apart surfaces with defined radii are associated with one of the components and cooperate with slots defined in the other of the components. A locking mechanism, e.g., a locking screw, may secure the components in a desired relative orientation.

The disclosure discloses methods, devices, systems and kits for repairing, replacing and/or augmenting natural facet joint surfaces and/or facet capsules. An implantable facet joint device of one embodiment comprises a cephalad facet joint element and a caudal facet joint element. The cephalad facet joint element includes a member adapted to engage a first vertebra, and an artificial cephalad bearing member. The caudal facet joint element includes a connector adapted for fixation to a second vertebra at a fixation point and an artificial caudal bearing member adapted to engage the cephalad bearing member. The artificial caudal bearing member is adapted for a location lateral to the fixation point. In another embodiment, an implantable facet joint device comprises a cephalad crossbar adapted to extend mediolaterally relative to a spine of a patient, the crossbar having opposite first and second ends, a connector element adapted to connect the crossbar to a first vertebra, a first artificial cephalad bearing member adapted for connection to the first end of the crossbar and adapted to engage a first caudal facet joint element connected to a second vertebra, and a second artificial cephalad bearing member adapted for connection to the second end of the crossbar and adapted to engage a second caudal facet joint element connected to the second vertebra.

An intervertebral implant component of an intervertebral implant includes an outer surface for engaging an adjacent vertebra and an inner surface. A keel extends from the outer surface and is designed to be disposed in a slot provided in the adjacent vertebra. This keel extends in a plane which is non-perpendicular to the outer surface; and preferably there are two of the keels extending from the outer surface which are preferably offset laterally from one another. In another embodiment, an anterior shelf is provided at an anterior end of the outer surface, and this anterior shelf extends vertically away from the inner surface in order to help prevent bone growth from the adjacent vertebra towards the inner surface. Further in accordance with disclosed embodiments, various materials, shapes and forms of construction of the component and/or keel provide various benefits.

A prosthetic implant replaces hyaline cartilage in a synovial joint with a flexible polymer sliding surface, preferably of hydrogel, on a segmented support with an array of adjacent segments to which the hydrogel is molded. Adjacent segments are laterally and angularly displaceable permitting the implant to conform to rounded or irregular surfaces or to be rolled or folded for arthroscopic placement. Tension cables threaded through segments along a circuit can cinch segments together for stiffening the supporting layer and/or the cable can pull the implant against a bone surface. Adjacent segments can have inter-engaged structures. In some embodiments the segments are carried on a flexible foil or fibrous sheet.

The present invention relates to a discal annular assistance device and the surgical instruments necessary for the insertion and removal thereof. This new device assists the annulus fibrosus following the exeresis of the nucleus pulposus of a lumbar intervertebral disc, to stop accelerated progression towards the discoligamentous instability of a vertebral unit operated on for a nucleus pulposus hernia.

An implant including a cage configured to be implanted between two vertebrae, including a first deployable keel, including a first blade, a first flange extending substantially perpendicularly from a first edge of the first blade, and a second flange extending substantially perpendicularly from a second edge of the first blade, such that the cross-section of the first deployable keel is in the shape of half of an I-beam. The implant further includes a second deployable keel, including a second blade, a third flange extending substantially perpendicularly from a first edge of the second blade, and a fourth flange extending substantially perpendicularly from a second edge of the second blade, such that the cross-section of the second deployable keel is in the shape of half of an I-beam. The first keel is configured to deploy in a superior direction, and the second keel is configured to deploy in an inferior direction.