A blade-like stem of a hip joint prosthesis for anchoring in the femur, including a prosthesis neck portion and a femur-anchoring portion extending therefrom and having a proximal end and a distal end, the femur-anchoring portion including a proximal arcuate portion extending from a location adjacent the proximal end and having a radius of curvature that changes in a distal-to-proximal direction, and the femur-anchoring portion further including a distal tapered portion extending from the proximal arcuate portion toward the distal end.

An intervertebral implant has a hollow space formed within the implant and accessible through an elongate opening extending through a recessed portion of the side wall, and the hollow space is shaped to receive an engagement portion of a drive shaft of an insertion tool; and the intervertebral implant includes at least two guiding surfaces facing each other and being configured for sliding engagement by a portion of a sleeve of the insertion tool movably holding the drive shaft.

A method includes generating a surgical plan for aligning a structure with a first bone segment and a second bone segment, and controlling a controllable guide structure to guide a cutting tool to sculpt the first bone segment, the second bone segment, and the structure based on the surgical plan. The method can include providing the first bone segment with a first bone mating surface by sculpting the first bone segment, providing the second bone segment with a second bone mating surface by sculpting the second bone segment, and providing, by sculpting the structure, the structure with at least one structure mating surface that is complementary to at least one of the first bone mating surface or the second bone mating surface.

Bone implant compositions and methods are provide that have an outer surface, the outer surface comprising demineralized bone and having a cavity disposed in the outer surface, the cavity having a demineralized bone material coated therein; and an inner surface of the bone implant comprising cortical bone, the inner surface contacting the outer surface. The bone implant compositions and methods provided are osteoinductive and allow rapid bone fusion.

A radiolucent intervertebral prosthesis is implanted in an environment that has been prepared in a manner which enhances radiopacity of the prosthesis and/or the environment. A liquid, powder, or other fluid radiopaque (RO) material, such as iohexol, is introduced into an implantation site, either by directly introducing the material into the site and/or by applying the material to a surface of the implant. The presence of the RO material in the implantation site provides contrast with the material of radiolucent prosthesis while the implantation site is being radiographically imaged, e.g. during fluoroscopic visualization while the prosthesis is being implanted. During implantation, the RO material helps the physician view and manipulate the implant, and after the implantation is complete, the RO material will be resorbed or otherwise lost from the implantation site so that the area returns to a radiolucent condition to facilitate subsequent radiographic imaging when needed.

A glenoid baseplate is provided that has a transverse body and an elongate body. The transverse body has a first side configured to engage scapula bone of a patient, a second side configured to face away from the first side, and a plurality of anchor apertures. The anchor apertures are formed between the first side and the second side. The transverse body also can have an arcuate or circular periphery that has an anterior portion configured to be oriented toward an anterior side of a scapula and a posterior portion that is configured to be oriented toward a posterior side of the scapula. The elongate body is disposed along a longitudinal axis between an end coupled with the first side of the transverse body. The longitudinal axis of the elongate body is off-set from the center of the circular periphery.

An intervertebral implant includes a body with a first face, a second face connected to the first face, and an axis of rotation. The body defines a hollow space for connecting to an insertion device, the hollow space being accessible through an opening formed between the first and second faces. The opening is elongate and extends around the axis of rotation to facilitate pivoting of the implant relative to the insertion device about the axis of rotation to a first angular position and a second angular position. The implant further includes a first abutment surface that engages the insertion device in a form-fit manner at the first angular position, and a second abutment surface that engages the insertion device in a form-fit manner at the second angular position. The opening can also engage the insertion device to hold the implant at least one additional angular position.

A glenoid baseplate is provided that has a transverse body and an elongate body. The transverse body has a first side configured to engage scapula bone of a patient, a second side configured to face away from the first side, and a plurality of anchor apertures. The anchor apertures are formed between the first side and the second side. The transverse body also can have an arcuate or circular periphery that has an anterior portion configured to be oriented toward an anterior side of a scapula and a posterior portion that is configured to be oriented toward a posterior side of the scapula. The elongate body is disposed along a longitudinal axis between an end coupled with the first side of the transverse body. The longitudinal axis of the elongate body is off-set from the center of the circular periphery.

Devices, systems and methods for surgical treatment of mid-foot disorders such as osteoarthritis, spacing disorders, or alignment disorders, including mid-foot arthroplasty devices and systems for the 2.sup.nd and 3.sup.rd tarsometatarsal (TMT) joint, implants for post-osteotomy spacing and realignment, arthroplasty articular implants, dowel grafts for TMT arthrodesis or fusion, dowel grafts for navicular cuneiform (NC) arthrodesis, dowel grafts for intercuneiform arthrodesis, and/or locking dowels for joint fusion.

An intervertebral implant has a hollow space formed within the implant and accessible through an elongate opening extending through a recessed portion of the side wall, and the hollow space is shaped to receive an engagement portion of a drive shaft of an insertion tool; and the intervertebral implant includes at least two guiding surfaces facing each other and being configured for sliding engagement by a portion of a sleeve of the insertion tool movably holding the drive shaft.