A glenoid assembly includes a base component having a humeral-facing side and a scapula-facing side, the base component defining a bearing surface defined on the humeral-facing side, a first peg extending from the scapula-facing side of the base component, the first peg including a first shaft with a first passageway extending through the first shaft, and a second peg extending from the scapula-facing side of the base component, the second peg including a second shaft with a second passageway extending through the second shaft, wherein the first peg and the second peg are positioned in non-parallel orientation with respect to each other.

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 there between. 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 joint replacement implant is disclosed. The implant includes a body having a bone contact surface and an articulation surface. An expandable stem extends longitudinally from the bone contact surface. The expandable stem includes a plurality of flanges. The plurality of flanges are expandable from a first diameter to a second diameter to anchor the implant to a bone.

An intervertebral implant component of an intervertebral implant includes an outer surface for engaging an adjacent vertebra and an inner surface. A keel extends from the outer surface and is designed to be disposed in a slot provided in the adjacent vertebra. This keel extends in a plane which is non-perpendicular to the outer surface; and preferably there are two of the keels extending from the outer surface which are preferably offset laterally from one another. In another embodiment, an anterior shelf is provided at an anterior end of the outer surface, and this anterior shelf extends vertically away from the inner surface in order to help prevent bone growth from the adjacent vertebra towards the inner surface. Further in accordance with disclosed embodiments, various materials, shapes and forms of construction of the component and/or keel provide various benefits.

A tibial baseplate may include a bridge portion connecting medial and lateral condylar portions at an anterior end portion of the baseplate, and a pair of fixation members extending inferiorly from a bone contacting surface of each of the medial and lateral condylar portions. One of each pair of fixation members may extend posteriorly from the bone contacting surface, may be positioned anterior to the other of the pair, and may include at least one recessed surface. The recessed surface may include a lateral recess, a posterior recess, and a medial recess. During insertion of the tibial baseplate into the bone, one of each pair of fixation members may guide the tibial baseplate into the bone and secure the tibial baseplate, while the other of each pair of fixation members may drag along the bone so that bone chips accumulate in the recesses, providing for increased fixation of the baseplate.

An intervertebral cage structure that comprises a main body having a first surface and a second surface located opposite to the first surface, a first plate disposed on the first surface of the main body, a second plate disposed on the second surface of the main body, and an opening formed at a center portion of the intervertebral cage structure and extending from the first plate to the second plate via the main body, wherein the first and second plates comprise a surface pattern comprising at least one of a symmetrical geometric pattern and an asymmetrical geometric pattern.

This invention is directed to orthopedic implants and systems. The invention also relates to methods of implant design, manufacture, modeling and implantation as well as to surgical tools and kits used therewith. The implants are designed by analyzing the articular surface to be corrected and creating a device with an anatomic or near anatomic fit; or selecting a pre-designed implant having characteristics that give the implant the best fit to the existing defect.

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 there between. 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.

In accordance with one aspect, a spinal implant for fusing vertebral bones is provided that includes a monolithic body for being inserted between bones. The body has a through opening of the body for receiving bone growth material and a wall of the body extending about the through opening. The wall includes nubs extending into the through opening that increase the surface area of the wall available for bone on-growth.

A method for securing a stemless humeral includes positioning the stemless humeral anchoring component to the humerus such that a lateral anchoring wing extends in a direction of a lateral side of the humerus into a lateral region and two medial anchoring wings face a medial side of the humerus in a medial region. The lateral region has a lower bone density relative to the medial region. The stemless humeral anchoring component is positioned eccentrically such that the anchoring stud and the two medial anchoring wings are anchored in the medial region. The stemless humeral anchoring component is secured in resected proximal epiphyseal and metaphyseal portions of the humerus without reaching a diaphyseal portion of the humerus.