Provided is a structure of a porous spinal implant including a cage body inserted between adjacent vertebral bodies and divided by an upper surface, a lower surface, a left surface, a right surface, a front surface, and a rear surface, a plurality of vertical pores formed on the upper surface and the lower surface of the cage body, and a plurality of horizontal structures stacked on the left surface and the right surface of the cage body, wherein the plurality of vertical pores and the plurality of horizontal structures are each formed in a pattern that repeats in up-down, left-right, and front-rear directions. The structure of a porous spinal implant is capable of reducing strength of a cage body close to that of a vertebral body.

An expandable intervertebral implant is disclosed for use in between adjacent vertebral bodies in a spine. An expandable intervertebral implant may include an upper plate having a first upper side and a second upper side, a lower plate having a first lower side, a second lower side, and a first lattice that connects the first upper side to the first lower side. The expandable intervertebral implant may further include a second lattice that connects the second upper side of the upper plate to the second lower side of the lower plate and an opening having a longitudinal axis between the upper plate, lower plate, first lattice, and second lattice. The expandable intervertebral implant may further include an expansion mechanism comprising a driver that expands the upper plate and the lower plate away from each other along a cephalad-caudal axis by deforming the first lattice and the second lattice.

A method of treating a patient in need of an orthopedic implant is described. The method includes obtaining the T-score or bone density of the patient's native bone at a site of implantation, said T-score or bone density being determined by a DEXA scan or other means of determining a T-score or bone density. The method further includes selecting an orthopedic implant that has about the same density as the native bone at the site of implantation, and implanting the orthopedic implant at the site of implantation.

A surgical device is provided. The surgical device includes a tubular outer shaft having a longitudinal axis and an angled guide positioned on a first end of the surgical device. The angled guide may be angled relative to the longitudinal axis of the outer shaft. The surgical device includes an elongated inner shaft having a second end and a third end. The inner shaft is removably coupled to the outer shaft and configured to axially translate through the outer shaft. The surgical device includes pivotal device having at least one joint and an access tool. The at least one joint may be pivotally coupled to the third end of the inner shaft and to an end of the access tool. The pivotal device may be configured to axially translate through the angled guide into a deployed position.

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.

At least one embodiment comprises a talus implant comprising: a body section; a neck section; a crown, wherein the crown is positioned at a top portion of the body section; at least one wing coupled to the body section, wherein the wing extends out from the body section. At least one embodiment further comprises at least one screw hole positioned in at least one of the neck section and the body section. In at least one embodiment the outer surface of the implant is polished. In at least one embodiment a portion of the outer surface is polished while a portion of the outer surface is roughened.

The invention discloses a bionic artificial hip joint. The artificial hip joint includes a femoral stem located above corpus femoris, and a convex force-bearing part is provided on the femoral stem. The force-bearing part abuts against the inner side of the cortex on greater trochanter and bears a part of the longitudinal stress; its hollow design is convenient for bone grafting, so that the prosthesis and the greater trochanter can be integrated. Replacement surgery can preserve the hard cortex on the greater trochanter, providing another focus point for the femoral stem and further improving the stability of the connection between the bionic artificial hip joint and corpus femoris.

A stand-alone ALIF implant that comprises a cage and a rotatable plate attached to an anterior portion of the cage by a fastener mechanism. The plate may also be integrally formed with the cage, and both are typically manufactured using additive manufacturing techniques. Support material may be added during the additive manufacturing process to lend support to the implant, and may be positioned around the fastener mechanism during manufacturing of the implant. Once formed, the support material may be dissolved away, thereby allowing the plate to rotate independently from the cage, but still remain movably attached via the fastener mechanism. The cage may further comprise webbing thereon to promote bone growth.

Embodiments of the present invention are directed to microscale and millimeter scale tissue scaffolding structures that may be static or expandable and which may be formed of biocompatible metals or other materials that may be coated to become biocompatible. Scaffold structures may include features for holding desired biological or physiological materials to enhance selected tissue growth. Scaffolding devices may be formed by multi-layer, multi-material electrochemical fabrication methods.

A medullary rod has a peripheral wall defining the outer shape of the medullary rod, and inwardly delimiting a hollow space. The medullary rod also has a plurality of first partitions. The first partitions are generally parallel to one another, extend between the inner side of the medullary rod located along the inner edge of the long bone after implantation, and the outer side of the medullary rod located along the outer edge of the long bone after implantation. Each of the first partitions is integral with the peripheral wall at these inner and outer sides of the medullary rod.