Provided is an implant for restoring the mobility of an articular end of a bone. The implant includes a framework having a first face and a second face opposite the first face, the framework is defined by a plurality of free volumes formed by a grating, where the grating includes a first series of bars extending through the framework from the first face to the second face, and a second series of bars extending through the framework from the first face to the second face, wherein the second series of bars are parallel to one another, and spaced apart in pairs, where the bars have ends along the second face that are bevelled.

Disclosed is a spinal complex cage, which includes a cage which is made of a polymeric material, and metal covers which are formed on upper and lower portions of the cage, respectively, in which couplers formed on the metal covers are coupled to coupling grooves formed in the cage, such that the metal covers are detachably coupled to the upper and lower portions of the cage. Accordingly, because the cage and the metal cover are detachably coupled to each other, the manufacturing method is simple, and the metal cover is easily coupled to or separated from the cage, such that the spinal complex cage may be variously and quickly applied even during the surgery in accordance with shapes or intervals between the vertebral bodies, and as a result, a spinal fusion rate is excellent, and the accurate and precise surgical operation is enabled.

A device for containing bone graft material includes a mesh outer sleeve extending longitudinally from a proximal end to a distal end and sized and shaped to correspond to a profile of an outer surface of a target bone. The outer sleeve includes a longitudinal slot extending along a length thereof. The device also includes a mesh inner sleeve connected to an interior surface of the outer sleeve via at least one strut so that a bone graft collecting space is defined therebetween. The inner sleeve is sized and shaped to correspond to a profile of a medullary canal of the target bone. In addition, the device includes an interstitial mesh extending radially away from an exterior surface of the inner sleeve toward an interior surface of the outer sleeve to hold graft material in the bone graft collecting space.

A porous coating for a medical implant, wherein the porous coating comprises a porous, shape memory material.

A composite interbody device includes (a) a plastic core having a superior surface and an inferior surface, (b) a superior endplate and (c) an inferior endplate. Each of the superior and inferior endplates includes (i) a bone interface side for interfacing with bone and having a plurality of pores permitting bone growth therein, and (ii) a core interface side, opposite the bone interface side, having a plurality of voids that accommodate material of the plastic core to couple the endplate to a respective one of the superior and inferior surfaces, wherein the voids are isolated from the pores to prevent the material of the plastic core from entering the pores.

A dynamic porous coating for an orthopedic implant, wherein the dynamic porous coating is adapted to apply an expansive force against adjacent bone so as to fill gaps between the dynamic porous coating and adjacent bone and to create an interference fit between the orthopedic implant and the adjacent bone.

An elastomeric artificial joint and prosthesis system combining motion preservation and shock absorption through the interaction of core and endplate components. The core is comprised of: ahub having congruent concavity with the endplate surface allowing for rotation, translation, flexion and extension, orbital, lateral bending, and compression motion similar to that of a joint or natural intervertebral disc; aflange attached to the hub and able to move congruently with the hub, and having negative spaces providing an internal structure for an elastomer; and a bio-compatible elastomer casted around and through the flange providing shock absorption. The endplate has a low-friction surface and engages the elastomer, and a structural component that engages the vertebral endplate or bone surface. The device has medical applications such as in total joint arthroplasty, disc replacement, and industrial applications such as in robotics that are modeled to move similar to human anatomical motion.

A method of manufacturing a composite interbody device includes assembling superior and inferior endplates, this including forming or layering micro-porous titanium on opposing sides of a solid titanium sheet. A first of the opposing sides provides a micro-porous bone interface layer and a second of the opposing sides provides a micro-porous core interface side. The solid titanium sheet therebetween forms a central barrier layer. The inferior and superior endplates are placed in a mold, on each side of a core cavity, with the core interface sides facing the core cavity and the bone interface sides facing away from the cavity. Molten plastic is injection-molded into the core cavity to form a plastic core between the endplates, the molten plastic extruding into pores of the microporous core interface sides. The plastic is set to bond the core with the endplates.

A prosthetic talus comprising: a base having a top surface and a bottom surface; and an articulating component having a top surface and a bottom surface, wherein the bottom surface of the articulating component is removably coupled to the top surface of the base, wherein the bottom surface of the articulating component includes a protrusion, and wherein the top surface of the base includes a recess configured to receive the protrusion to thereby removably couple the articulating component to the base, wherein the articulating component includes a sidewall positioned between the top surface and the bottom surface, and wherein the sidewall includes a plurality of holes.

A process for printing a talus implant comprising the steps of scanning a joint for a damaged talus, and scanning a contralateral joint for a healthy talus. Next, the process includes obtaining dimensions for a talus based upon an initial scan and then obtaining dimensions for a talus based upon the scan of the contralateral joint. Next the process includes inverting the dimensions of the talus in the contralateral joint and then comparing the dimensions of the calculated talus with a pre-set of dimensions in a database. Next the process includes exporting a set of dimensions to a printer to print a talus implant.