A system and method for providing a spinal implant having a main body, a proximal anchor, a distal anchor, and an internal plunger. The proximal anchor comprises a nut having an internal bore. The distal anchor comprises a plurality of wings having a first closed configuration and a second open configuration. The internal plunger is housed within a central bore of the main body. The distal end of the internal plunger is operatively connected to the first wing and the second wing to selectively move the wings between the first closed configuration and the second open configuration, and vice versa.

An intervertebral disc prosthesis (1) having at least one upper plateau (4, 4′) and at least one lower plateau (5, 5′), which are separated by two movable cores (6, 6′) whose lower face (62, 62′) and upper face (61, 61′) respectively match a concave surface (54, 54′) of the upper plateau (4, 4′) and a convex surface (44, 44′) of the lower plateau (5, 5′). An intervertebral prosthetic unit (10) is also described having an intervertebral disc prosthesis and a posterior articular prosthesis (11) provided with two adjacent and partially tangent articular blades (12, 13), which are each coupled to a vertebra (3, 3′) by coupling devices (14) and are connected by guide devices that allow them to move along a curve whose center C3 is provided on the same side as the implantation of said coupling means.

A system for spinal surgery includes a prosthesis comprising a plurality of bone anchors which engage an intervertebral construct for fusion or motion preservation. The fusion construct comprises a spacer optionally encircled by a jacket. The motion preservation construct may comprise an articulating disc assembly or an elastomeric disc assembly. Any of the constructs may occupy the intervertebral disc space between adjacent vertebrae after removal of an intervertebral disc. The anchors slidingly engage the construct to securely fix the prosthesis to the vertebrae. The anchors and jacket of the fusion construct provide a continuous load path across opposite sides of the prosthesis so as to resist antagonistic motions of the spine.

A special tube is disclosed for the insertion of materials inside the maxillary sinus in order to displace the Schneiderian membrane. The tube is connected to a source of a flowable material. The tube is inserted through the alveolar ridge beneath the maxillary sinus and when the flowable material is advanced through the tube the Schneiderian membrane is lifted. The tube can be part of a dental implant which is screwed inside the alveolar ridge.

An artificial joint cup (2), in particular a hip joint cup, for implanting in a cavity in a bone. The joint cup (2) is, in particular, substantially in the form of a spherical dome cup, having a convex outer surface (3) and a concave inner surface (4). In addition, the joint cup (2) comprises an outer diameter (OD) and an inner diameter (ID). The ratio of the difference (D) between the outer diameter (OD) and the inner diameter (ID) in relation to the outer diameter (OD) is in a region between 0.5 and 0.07, preferably between 0.3 and 0.075, particularly preferably between 0.2 and 0.1. The joint cup (2) is manufactured from a ceramic material, and the convex outer surface (3) has a micro-structuring.

An intervertebral disc includes a superior endplate having an upper vertebral contacting surface and a lower bearing surface, wherein the upper vertebral contacting surface of the superior endplate has a central portion that is raised relative to a peripheral portion of the superior endplate, and wherein the lower bearing surface has a concavity disposed opposite the raised central portion. The disc includes an inferior endplate having a lower vertebral contacting surface and an upper surface, wherein the lower vertebral contacting surface of the inferior endplate has a central portion and wherein the upper bearing surface has a concavity disposed opposite the central portion. A core is positioned between the upper and inferior endplates, the core having upper and lower core bearing surfaces configured to mate with the bearing surfaces of the upper and inferior endplates. The upper vertebral contacting surface of the superior end plate has a different shape than the lower vertebral contacting surface of the inferior end plate.

A facet joint replacement system includes an inferior implant with an inferior articular surface, a superior implant with a superior articular surface and may include a crosslink extending across a vertebral sagittal plane. The inferior implant may comprise an inferior strut, and a polyaxially adjustable, lockable mechanism which may couple the inferior articular surface with a first end of the inferior strut, and couple the inferior articular surface with the crosslink. A second end of the inferior strut may be secured to a polyaxially adjustable, lockable fixation assembly securable in a vertebra. The superior implant may be secured to a polyaxially adjustable lockable fixation assembly securable in a vertebra. The positions of the inferior articular surface and the first end of the inferior strut are independently translatable along a medial-lateral axis of the vertebra prior to lockout by the lockable mechanism. The crosslink may be placed into the lockable mechanism from a posterior approach.

A modular humeral implant for an inverted shoulder prosthesis includes a humeral stem having, on the one hand, a diaphyseal keel of elongate shape, extending along a diaphyseal axis and shaped to be engaged in a medullary cavity of a humerus, and, on the other hand, a metaphyseal portion. A humeral spacer is mounted on the metaphyseal portion of the humeral stem and has a lower face facing the metaphyseal portion, the lower face having a peripheral portion projecting laterally from the metaphyseal portion and covered at least partially with a porous or rough metal surface coating promoting an osseointegration. A humeral insert is fastened on the humeral spacer and has a hemispherical cup shaped to receive a glenosphere of a glenoid implant.

Endosseous implant to be applied to a human or animal bone, wherein the surface of the implant is made from titanium or a titanium alloy, said implant having a smooth or rough surface texture, which is characterized in that said surface has been treated with at least one selected organic phosphonate compound or a pharmaceutically acceptable salt or ester or an amide thereof; process for producing said implants.

A spinal cage with a wall extending in a longitudinal direction defining an interior space is disclosed. There is also provided a deployable element in movable relation to the spinal cage.