An implant including a housing having a peripheral frame including an inner edge defining central opening in a central portion of the implant. The implant may also include a blade located within the central opening, the blade having a retracted position in the housing and an extended position where the blade extends outwardly from the housing. In addition, the implant may include a blade actuating component comprising a driven shaft portion and a blade engaging portion. The blade actuating component may be configured to be translated to move the blade between the retracted position and the extended position. Also, the inner edge of the peripheral frame may include a posterior edge configured to support the blade in two locations.

An artificial joint implant (1) comprising a first element (2) with a socket (4) and a second element (3) with a ball head (5), wherein said ball head (5) is insertable in said socket (4) such as to form a ball-and-socket connection between said first element (2) and said second element (3), and the movement of said ball head (5) in said socket (4) is restricted by means of a protrusion (6.1; 6.2) engaged in a groove (7), whereby said protrusion (6.1; 6.2) has a central axis A2 and is protruding from the surface of said socket (4) and said groove (7) is provided on the surface of said ball head (5) or vice versa; said groove (7) is positioned along a great circle of said ball head (5) or of said socket (4), said protrusion (6.1; 6.2) has a shape allowing rotation of the protrusion around its central axis A2 when received in the groove (7); andthe surface roughness of the protrusion (6.1; 6.2) and/or of the groove (7) is at most 25 micrometers.

Method and set of surgical instruments for fitting a shoulder prosthesis, and the shoulder prosthesis. The proposed method seeks to interpose a bone graft between the previously prepared glenoid surface (G) of a scapula (S) of a patient's shoulder and the face of a glenoid prosthetic component opposite the articular surface. The set of instruments permit the bone graft to be taken from the upper epiphysis of the humerus (H), either in situ or ex vivo.

A methodology for grafting together adjacent bony structures is provided using an implant device having an endplate with an inner disc portion and outer ring portion spaced from the inner disc portion by a connecting wall disposed therebetween. An endplate interior surface includes a retaining structure for securing the endplate to one of the bony structures, and endplate an exterior surface has an integrally formed socket. A ball-joint rod has a longitudinally extending body and an end, and at least a portion of the ball-joint rod end is curvilinear in shape. The curvilinear ball-joint rod end is rotatably disposed in the endplate socket to fixedly interconnect the bony structures.

A system and method for transmitting implant data includes an orthopaedic implant, a wireless receiver, and a processing circuit electrically coupled to the wireless receiver. The orthopaedic implant is configured to transmit implant identification data and implant sensor data to the wireless receiver in response to a power signal. The orthopedic implant may transfer the data over, for example, a wireless network. The processing circuit receives the implant identification data and the implant sensor data from the wireless receiver and is configured to retrieve patient-related data from a database based on the implant identification data. The processing circuit may also be configured to update a patient queue, assign a patient room to a patient, and/or transmit the patient-related data and the implant sensor data to a client machine located in the patient room.

A methodology for grafting together adjacent bony structures is provided using an implant device having an endplate with an inner disc portion and outer ring portion spaced from the inner disc portion by a connecting wall disposed therebetween. An endplate interior surface includes a retaining structure for securing the endplate to one of the bony structures, and endplate an exterior surface has an integrally formed socket. A ball-joint rod has a longitudinally extending body and an end, and at least a portion of the ball-joint rod end is curvilinear in shape. The curvilinear ball-joint rod end is rotatably disposed in the endplate socket to fixedly interconnect the bony structures.

An intervertebral implant includes a core member operably coupled between an upper and a lower base member. An outer cavity extends between the core member upper end and lower end, and radially between the inner cavity and an outer surface of the core member. A core member inner wall is formed between the inner and an outer cavity, and a core member outer wall is formed between the outer cavity and the outer surface of the core member. A first locking member is positioned on at least one of the core member upper end and the core member lower end and at least one second locking member is positioned on an inner surface of at least one of the upper and lower base member for locking engagement. The upper and lower end of the core member are oriented at a lordotic angle ranging from 1 degrees to 20 degrees.

A methodology for grafting together adjacent bony structures is provided using an implant device having an endplate with an inner disc portion and outer ring portion spaced from the inner disc portion by a connecting wall disposed therebetween. An endplate interior surface includes a retaining structure for securing the endplate to one of the bony structures, and endplate an exterior surface has an integrally formed socket. A ball-joint rod has a longitudinally extending body and an end, and at least a portion of the ball-joint rod end is curvilinear in shape. The curvilinear ball-joint rod end is rotatably disposed in the endplate socket to fixedly interconnect the bony structures.

An artificial functional spinal unit including an expandable intervertebral implant that can be inserted via a posterior surgical approach and used with one or more facet replacement devices to provide an anatomically correct range of motion is described. Lordotic and non-lordotic expandable, articulating implants and cages are described, along with embodiments of facet replacement devices and instruments for insertion. Methods of insertion are also described.

A spacer formed of an intermetallic compound, such as nitinol. The spacer includes at least two segments shaped in opposing arches. The unique properties of the intermetallic compound enable the material to be deformed into a planar, insertable shape when the material is cooled below a transition temperature and returns to the undeformed shape when the material returns to an ambient, operational temperature. An expansion mechanism assembly engages with the spacer to apply an expansion force, extending the spacer longitudinally drawing the spacer into the planar configuration. The expansion mechanism assembly can be used to guide the spacer into the desired position within the patient. The spacer control mechanism assembly is subsequently removed, relieving the expansion force, returning the spacer to the natural un-deformed, arched shape as it returns to body temperature. Retention features can be integrated in the spacer to aid in retaining the spacer in location.