Disclosed is an endoprosthesis for implantation in bone surgery, in particular hip surgery, without the use of surgical cement. The hip joint endoprosthesis for implantation in bone surgery of ball-and-socket joints, in particular hip joint, has a moving connection provided by the contact surface of two modules of the endoprosthesis femoral head and acetabulum, whereas their surfaces which are in contact with the bone next to the joint have a shape similar to a sphere, on which pins are placed, with an axis principally parallel to the lengthwise axis of the endoprosthesis, and at least two cutting blades with an arc-shaped cross-section outline, creating a groove for removal of the products of cutting.

An expanding, conforming interbody implant includes a plurality of superior and a plurality of inferior segments. The segments are adapted to individually expand, contact, and conform to endplates of vertebral bodies to distribute forces equally over the implant and across the vertebral endplates. Once a proper extension of the segments has been achieved, the segments are locked in position. The implant has a stiffness that approximates the stiffness of bone, and the implant minimizes problems with subsidence, endplate fractures, and stress shielding.

In one embodiment, an intervertebral implant includes a body and a locking element. The body includes a leading surface and a trailing surface opposite the leading surface. The body also includes first and second bone fastener passageways through the implant body and a cavity in between the first and second passageways. The cavity includes a trailing wall that separates the cavity from the trailing surface. The locking element is disposed in the cavity such that part of the locking element is visible through an access opening in the trailing wall so that the locking element may be rotated from outside of the implant. In a first rotational position, a first part of the locking element is located within one of the first and second passageways and in a second rotational position, the first part of the locking element is inside the body covered by the trailing wall.

A partial ankle prosthesis includes a tibial component including a superior surface configured to be attached to a lower end of a patient's tibia; a poly component that is fixedly attached to the tibial component and includes a concave inferior surface of an anti-friction material; and a talar component including an inferior surface configured to be attached to a patient's talus and a single convex superior surface configured to mate with the inferior surface of the poly component; and the partial ankle prosthesis is configured to be implanted in a single compartment of a patient's ankle.

An approach is provided for a three-dimensional (3D) printing method for forming a 3D object. The approach provides for printing a structure of the 3D object by depositing a thermoplastic material, in which the thermoplastic material is radiolucent. The approach provides for printing one or more radio-opaque markers by depositing another material, which includes at least a radio-opaque material. The approach integrates the one or more radio-opaque markers with the structure of the 3D object.

The present disclosure provides for spinal implants configured for lateral insertion techniques deployable between a contracted position and an expanded position. The spinal implant may include a first endplate and a second endplate, each having a plurality of guide walls and inclined ramps. The spinal implant may further include a moving mechanism having first and second trolleys configured to act against the first and second plurality of ramps. The moving mechanism may further include a first set screw and a second set screw opposite the first set screw. The moving mechanism may be configured to operably adjust a spacing between the first and second endplates upon simultaneous rotation of the first and second set screws along a rotation axis, and may also operably adjust an angle of inclination between the first and second endplates upon rotating the first set screw or second set screw along the rotation axis.

Spinal implants that are configured for a minimally invasive approach to a patient's intervertebral disc space, optimized to avoid blood vessels and nervous tissue, maximizing endplate coverage and promoting sagittal balance, are provided. Insertion and fixation can be accomplished through a narrow access window, thereby allowing better access to more spinal levels while being less invasive than other approaches. The spinal implants may facilitate fusion, and include visualization features to assist in the implantation and verify proper placement and vary segmental angle of lordosis. Methods of implanting the spinal implants to treat a patient's spine are also disclosed.

An anchoring fixture for anchoring a prothesis to a skull bone may comprise a screw thread apparatus including a screw thread having a varying outer diameter and formed along a longitudinal length of the anchoring fixture; a flange configured to function as a stop for the anchoring fixture adapted to rest on top of the bone when the anchoring fixture is implanted into the bone; at least a main relief chamber formed into a portion of the screw thread having a first side along the longitudinal length that is curved shaped, and wherein the anchoring fixture is tapered over at least a first portion of the longitudinal length of the anchoring fixture and where the first portion is arranged at a distal end of the anchoring fixture, and where the distal end is opposite to the flange.

The present invention disclosed a method of producing a three-dimensional porous tissue in-growth structure. The method includes the steps of depositing a first layer of metal powder and scanning the first layer of metal powder with a laser beam to form a portion of a plurality of predetermined unit cells. Depositing at least one additional layer of metal powder onto a previous layer and repeating the step of scanning a laser beam for at least one of the additional layers in order to continuing forming the predetermined unit cells. The method further includes continuing the depositing and scanning steps to form a medical implant.

Implants for vertebral body or functional spinal unit replacement comprise a bioactive surface roughening on one or more of the anterior, posterior, and lateral surfaces of the implant. The bioactive surface includes macro-, micro-, and nano-scale structural features that contact vertebral bone that lines a specialized channel in a vertebrae, and thereby facilitate bone growth and osteointegration of the implant with the vertebral bone.