An implant assembly is shown and described. The implant has at least one or a plurality of elastic, resilient or flexible arms that each have a detent adapted to retain at least one screw in a locked position in the implant. At least one of the arms has a portion that extends into a screw aperture such that an arm axis is generally parallel to the axis of the screw after the screw is received in the implant. In another embodiment, means or a system for locking the multi-component implant members together is shown.

The invention provides a method of making a biological disc graft. In one embodiment, the biological disc graft is useful for treating back or neck pain. In one embodiment, the biological disc graft is useful for treating any joint pain. The invention also provides a method of implanting said biological disc graft in a way that is minimally invasive and less dangerous.

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.

The invention makes available a multi-part implant (10), comprising: a support element (20) for fixing the implant (10) to a bone material; wherein the support element (20) forms a receiving space; and a functional element (30) that can be introduced into the receiving space; wherein the functional element (30) can be fixed in the receiving space (26) by the support element (20) at least with respect to one degree of freedom.

A problem with total disc implant surgery appears to be the positioning of the implant which if not correct may lead to pain and eventually new surgery. The present invention relates to an improved disc implant for total disc replacement, that includes two inter-vertebral elements which are flexibly connected via a coupling mechanism. Following surgery, the relative movability of the two inter-vertebral elements is decreased overtime, as bone ingrowth occurring around the implant and specifically through osseointegrative sections gradually decrease the movability of the elements relative to each other. Following, the relative movability of the implant elements is replaced by fixation of the elements. The fixation has flowingly occurred in a position affected by the movement of the patient, and is thereby more acceptable to the patient.

A method of placing an implant for intervertebral fusion between adjacent vertebral bodies in a patient includes inserting the implant in a space between the adjacent vertebral bodies such that both a first intervertebral spacer body and a second intervertebral spacer body contact each of the adjacent vertebral bodies. The first intervertebral spacer body is spaced apart from the second intervertebral spacer body. An expandable container portion of the implant disposed between the first intervertebral spacer body and the second intervertebral spacer body is filled with fill material such that the expandable container expands to contact each of the adjacent vertebral bodies.

The present application is generally directed to implantable systems, devices and related methods pertaining to spinal surgery. In particular, the present application discloses a frame and spacer system for inserting into a disc space. The frame and spacer system is of low profile. The frame can receive different fixation devices, including threaded and non-threaded fixation devices.

An implant assembly is shown and described. The implant has at least one or a plurality of elastic, resilient or flexible arms that each have a detent adapted to retain at least one screw in a locked position in the implant. At least one of the arms has a portion that extends into a screw aperture such that an arm axis is generally parallel to the axis of the screw after the screw is received in the implant. In another embodiment, means or a system for locking the multi-component implant members together is shown.

The shoulder prosthesis component comprises an implantation body, which defines an implantation axis and which is designed to be received within a bone of a patient that includes a cortical bone external layer and a cancellous bone internal layer, and to compact therein the cancellous bone internal layer in a planned manner that is differentiated along and around the implantation axis depending on preoperative local bone density and quantity of the cancellous bone internal layer. A method for producing such a shoulder prosthesis component for a patient is also proposed.

An expandable spacer, comprising: an axial tube having a surface, a proximal end and a distal end and a length, wherein, said surface defines a plurality of slits, said plurality of slits defining at least two axially displaced extensions, such that when said tube is axially compressed, said extensions extend out of said surface and define a geometry of an expanded spacer. Preferably the spacer is adapted to be inserted between two spinal vertebrae of a human.