Disclosed is a cage which is inserted between vertebral bodies of a cervical vertebra or spine during an operation for treating a cervical disc disease, myelosis, or fracture of the cervical vertebra or spine, and more particularly, to a cage with spikes, including upper and lower spikes which are attached to a clip inserted into a main body of the cage, unfolded upward and downward from the main body, and locked to vertebral bodies of a cervical vertebra or spine positioned at the top and bottom of the cage such that the cage is fixed and locked between the vertebral bodies.

Implant assemblies, systems, and methods for stabilizing a joint between a superior vertebra and an inferior vertebra may include a plate member coupled to an interbody spacer with at least one fastener that extends superiorly or inferiorly from the implant assembly to anchor within a vertebral body and stabilize the joint. Inserters and methods of insertion may also be included to facilitate fixation of various implant assemblies within the intervertebral space of the joint between the superior vertebra and the inferior vertebra.

Embodiments are directed to a spinal implant device for reducing effects of a spinal disc herniation that includes a support frame, where the support frame has a first end, a second end, and a mounting hole for receiving a fastener that attaches the support frame to a vertebra, and a cushion attached to the support frame. Embodiments are also directed to a system for implanting a medical device to a spine that includes a spinal implant device having a support frame, where the support frame has a first end, a second end, and a mounting hole, and a cushion attached to the support frame. The system also includes a fastener for attaching the spinal implant device to a vertebra, where the spinal implant device is moveable to align the cushion to a disc space created after a portion of a herniated disc is removed during surgery.

In some embodiments, the present disclosure relates to a system that includes an insertion tool and a drill guide. The insertion tool includes a body with a distal portion and a distal end. The body has a first engagement feature extending longitudinally along the distal portion and two arms extending longitudinally from the distal end of the body. The drill guide includes two bores and an open faced channel therebetween. The open faced channel includes a second engagement feature slidably engageable with the first engagement feature on the body of the insertion tool. The two bores are adapted for the disposal of a fastener driver tool therethrough.

The present invention relates to a vertebral implant, in particular for corpectomy, to a device for attaching a vertebral implant and to implantation instrumentation, the implant including at least one first body (2) and at least one second body (3) each having at least one face having shapes and dimensions mating those of at least one face of another body (3, 2) and forming mutual fitting means, in order to allow assembling of said bodies (2, 3) by sliding along a sliding axis and, on the other hand, at least one locking means (4) retained in at least one of the bodies (2, 3) and at least one abutment portion of which is laid out for passing from a so-called open position, allowing sliding for the assembling of said bodies (2, 3), to a so-called closed position, locking said bodies (2, 3) assembled together by the contact between at least said abutment portion and at least one abutment (42, 43) of at least one of said bodies (2, 3), said abutment (42, 43) being oriented not parallel to the sliding axis and said abutment portion passing from the open position to the closed position elastically by flexure or torsion.

An expanding interbody includes a first articulating member; a second articulating member rotatably connected to the first articulating member; and a clip member that engages each of the first articulating member and the second articulating member, wherein any of the first articulating member and the second articulating member includes a plurality of grooves arranged in a progressively elongated arrangement, and wherein the clip member includes at least one protruding tip that sequentially engages the plurality of grooves causing the first articulating member to rotate with respect to the second articulating member.

The present invention relates to a knee joint endoprosthesis having a tibial component and a femoral component and a hinge joint for coupling the tibial component and the femoral component so as to be pivotal about a rotational axis, which hinge joint comprises a first joint element and a second joint element coupled therewith so as to be rotatable about the rotational axis, wherein a connecting device is provided having at least one first connecting element and at least one second connecting element for connecting the first joint element to the femoral component, which connecting device defines a connecting position, in which the at least one first connecting element and the at least one second connecting element are engaged in a at least one of non-positive- and positive-locking manner, and an assembly position, in which the first joint element and the femoral component are fully separated from each other.

A reversible bone coupling device including a first component having a first elongated stem portion for insertion from a first end longitudinally into a surface of a first bone piece, and a second component having a second elongated stem portion for insertion from a second end longitudinally into a surface of a second bone piece, and a connector extending from a second top for coupling with the first component and reversibly locking therein.

A method of implanting a prosthetic stemless shoulder implant may include making an incision into a patient's shoulder area of a patient and passing a cutting instrument through a rotator cuff interval of the patient. A central portion of the native humeral head may be resected and removed so that a central void remains. The same or another cutting instrument may be inserted through the rotator cuff interval and into the central void. Medial and lateral portions of the native humeral head adjacent the central void may be resected and removed. A base of a prosthesis may be implanted into a proximal portion of the humerus after passing the base through the rotator cuff interval, and two humeral head portions may be inserted through the rotator cuff interval and coupled to the base and to one another.

Implant assemblies, systems, and methods for stabilizing a joint between a superior vertebra and an inferior vertebra may include a plate member coupled to an interbody spacer with at least one fastener that extends superiorly or inferiorly from the implant assembly to anchor within a vertebral body and stabilize the joint. Inserters and methods of insertion may also be included to facilitate fixation of various implant assemblies within the intervertebral space of the joint between the superior vertebra and the inferior vertebra.