An augment device for a joint endoprosthesis, the device including a sleeve surrounding a channel extending through the sleeve. The sleeve is formed of porous material for ingrowth of bony material, the sleeve comprising an inner face and an outer face. The sleeve further comprises a wall surrounding the channel, the wall being made of solid material and forming a sandwich structure with the porous material, wherein the wall forms a bulkhead between the inner face and the outer face. Thereby, the bulkhead wall will stop inflow of any cement across the sleeve from its inner to its outer face. The porous material on the outer face will be kept free from cement and its capability to promote bone ingrowth is reliably preserved. The augment devices are preferably provided as a set having different sizes and straight or stepped bottoms for improved versatility and maximum preservation of natural bone matter.

The biocompatible lattice structures disclosed herein with an increased or optimized lucency are prepared according to multiple methods of design disclosed herein. The methods allow for the design of a metallic material with sufficient strength for use in an implant and that remains radiolucent for x-ray imaging.

The intervertebral fusion device (200) comprises a superior component (220), an inferior component (240) and a core component (260). The superior and inferior components (220, 240) are received in an intervertebral space between first and second vertebrae whereby the superior component top side abuts against the first vertebra, the inferior component bottom side abuts against the second vertebra, and the superior component bottom side and the inferior component top side oppose each other. A height of the intervertebral fusion device is determined upon insertion of the core component (260) between the superior and inferior components (220, 240). Each of the superior component top side and the inferior component bottom side is one of: oblong having a major axis; and square, being bounded by four edges. During insertion of the core component (260) a first core profile of the core component cooperates with a superior component profile at the superior component bottom side and a second core profile of the core component cooperates with an inferior component profile at the inferior component top side whereby the core component moves in a direction oblique to the major axis where the superior component top side or the inferior component bottom side is oblong or to an edge of the superior component top side or the inferior component bottom side where the superior component top side or the inferior component bottom side is square.

A kit includes a distractor, a plurality of trial elements, and at least one sensor. The distractor is configured to separate a first bone from a second bone by adjusting the distance between a first member and a second member, and is configured to receive at least one sensor in the first portion. Each of the trial elements corresponds to one of a plurality of surgical implants, is configured to be temporarily coupled to the second bone so as to evaluate suitability of the corresponding one of the plurality of surgical implants for implantation, and is configured to receive at least one sensor. The at least one sensor is configured to be received in the distractor or one of the trial elements, and is configured to record a magnitude of a force, a direction of application of a force, a pressure mapping, or a location of application of a force.

An expandable implant includes a top support assembly defining an upper surface configured to engage a first portion of bone, a first central aperture extending from the upper surface to an interior of the implant, and a first grid structure surrounding the first central aperture; a bottom support assembly defining a lower surface configured to engage a second portion of bone, a second central aperture extending from the lower surface to the interior, and a second grid structure surrounding the second central aperture; and a control assembly coupled to the top support assembly and the bottom support assembly and configured to control relative movement between the top support assembly and the bottom support assembly between a collapsed position and an expanded position.

The present invention relates to a vertebral system comprising a vertebral implant (2) and a plurality of inserts, said implant being designed to be implanted in a vertebral segment composed of at least two vertebrae and including a body (20) the walls whereof delimit a cavity (23) leading to the outside of the body (20) through at least one opening in at least one of said walls, at least one passage (21) passing through the implant (2) from the periphery to an upper or lower surface to receive a bone-anchoring device (1) capable of anchoring the implant (2) in at least one of said vertebrae, the system being characterized in that it includes at least two inserts selected from among the following inserts: at least one graft insert (3, 3A, 3B, 4, 5A, 5B, 6A, 6B, 6C, 6D, 202, 250) capable of being colonized by bone tissue and/or receiving at least one bone tissue graft and/or at least one substitute: and/or at least one bone-anchoring insert (210) comprising said passage (21) capable of receiving said bone-anchoring device (1).

The present invention relates to an intervertebral fusion device (10) comprising a superior component (20), an inferior component (40), and a core component (80) inserted there between. The intervertebral fusion device further comprises first and second retention mechanisms which resist ejection of the core component from between the superior and inferior components. Each of the first and second retention mechanisms comprises first and second portions. One of the first and second portions is unitary with one of the superior and inferior components. The other of the first and second portions is unitary with the core component. The first and second portions each comprise an inter-engaging formation which are urged in an opposite direction. The first inter-engaging formation is urged to inter-engage with the second inter-engaging formation upon insertion of the core component between the superior and inferior components.

The present invention relates to an intervertebral fusion device (10) comprising a superior component (20), an inferior component (40) receivable in an intervertebral space between first and second vertebrae, with the core component (80) insertable between the superior and inferior components to determine a separation between the superior and inferior components. The superior, inferior components and core components comprise respective formations and profiles. The formations (54, 68) present a barrier to separation of the core from one of the inferior and superior components during insertion of the core component. The profiles guide the core component during insertion of the core component while presenting no barrier to separation from each other during its insertion. The components comprise further formations (39, 76) which present a barrier to separation of the components from each other once the core has been fully inserted between the inferior and superior components.

An augment device for a joint endoprosthesis, the device including a sleeve surrounding a channel extending through the sleeve. The sleeve is formed of porous material for ingrowth of bony material, the sleeve comprising an inner face and an outer face. The sleeve further comprises a wall surrounding the channel, the wall being made of solid material and forming a sandwich structure with the porous material, wherein the wall forms a bulkhead between the inner face and the outer face. Thereby, the bulkhead wall will stop inflow of any cement across the sleeve from its inner to its outer face. The porous material on the outer face will be kept free from cement and its capability to promote bone ingrowth is reliably preserved. The augment devices are preferably provided as a set having different sizes and straight or stepped bottoms for improved versatility and maximum preservation of natural bone matter.

The methods disclosed herein of generating three-dimensional lattice structures and reducing stress shielding have applications including use in medical implants. One method of generating a three-dimensional lattice structure can be used to generate a structure lattice and/or a lattice scaffold to support bone or tissue growth. One method of reducing stress shielding includes generating a structural lattice to provide sole mechanical spacing across an area for desired bone or tissue growth. Some examples can use a repeating modified rhombic dodecahedron or radial dodeca-rhombus unit cell. Some methods are also capable of providing a lattice structure with anisotropic properties to better suit the lattice for its intended purpose.