The present invention relates generally to a prosthetic spinal disc for replacing a damaged disc between two vertebrae of a spine and methods for inserting said discs. The intervertebral prosthetic discs are provided with connections for facilitating implantation and removal and features which enhance primary and secondary stability over time.

Augmentation material having a wire and, in axial alignment along the wire, a plurality of groups of axially adjacent connecting elements that extend radially from the wire, wherein the connecting elements are designed such that, when a first group from the plurality of groups is pressed together with a further group from the plurality of groups, the connecting element of the two groups can be connected to one another in a positive-locking and/or friction-locking manner.

Proposed is a spinal cage. The spinal cage includes a bone support portion configured to be disposed between a first vertebra at an upper side and a second vertebra at a lower side to support the first vertebra, a base portion positioned at a lower side of the bone support portion to come in contact with the second vertebra, and a sidewall portion which has an upper side end connected to an edge of the bone support portion and a lower side end connected to an edge of the base portion and includes an elastic band having elasticity and inelastic bands having relatively lower elasticity or no elasticity. Therefore, subsidence of the spinal cage into vertebrae can be suppressed.

A talar implant having at least one body section, at least one mesh section and at least one solid section extending down from the body section. The solid section having at least one point end. Further disclosed is a kit for inserting a talar implant including at least one tibial guide, at least one talar guide, and at least one impactor for inserting the talar implant into a talus. In addition, a method for implanting a talus implant is disclosed. The method can include identifying a damaged area on a talus, projecting a missing damaged area on a contralateral joint and printing an implant based upon a mirror image of a portion of the contralateral joint. The method can include applying at least one guide, removing at least a portion of a damaged region of the talus, inserting the talar implant and setting the talar implant in the talus.

There is disclosed a talus implant comprising a base having at least one hole and at least one pin. There is also a top comprising at least one hole and at least one pin, wherein the top is configured to be inserted into the base. At least one embodiment comprises a tibial implant comprising at least one post and at least one base coupled to the at least one post. Additionally, there is at least one pad coupled to the at least one base, wherein the at least one pad is selectively insertable into and removable from the at least one base. A method for fabricating a talus and tibial implant is disclosed and also a method for inserting a talus implant and a tibial implant into a patient having a damaged talus joint.

Implants, systems, instruments, methods, and kits for metatarsophalangeal joint arthroplasty may include metatarsal arthroplasty implants, repositioning guides, broach tools, inserter tools, and sterilizable packaging configured to facilitate metatarsal arthroplasty surgical procedures. The metatarsal arthroplasty implants may generally include an articular member having a convex articular surface, a concave bone-facing surface opposite the convex articular surface, and at least one side surface intermediate the convex articular surface and the concave bone-facing surface, as well as a central shaft sized for insertion into a metatarsal bone having a central shaft longitudinal axis, a central shaft proximal end coupled to the concave bone-facing surface of the articular member, and a central shaft distal end extending away from the concave bone-facing surface of the articular member along the central shaft longitudinal axis.

An expandable bi-dimensional intervertebral implant for an intervertebral fusion is provided. The implant includes a first hinge arm, a second hinge arm connected to the first hinge arm, and a translation member movable relative to the first hinge arm and the second hinge arm between an initial position and an engaged position. The second hinge arm is movable between a primary position and a secondary position relative to the first hinge arm. In the engaged position, the translation member biases the first hinge arm to move from a first position to a second position and biases the second hinge arm to move between a first position and a second position.

An orthopaedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient’s knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient’s knee to receive the implants. A number of methods for using the surgical instruments to prepare the bones is also disclosed.

An orthopaedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient's knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient's knee to receive the implants. A number of methods for using the surgical instruments to prepare the bones is also disclosed.

Embodiments described include devices and methods for forming a porous polymer material. Devices disclosed and formed using the methods described a spacer for spinal fusion, craniomaxillofacial (CMF) structures, and other structures for tissue implants.