Non-load-bearing, drug-eluting components, such as a rod cover, that can be added to load bearing spinal implants.

The present disclosure includes fixation devices, such as an orthopedic screw or implant, that comprises one or more porous elements or fenestrations to aid in osteo-integration of the fixation device. The fixation device may be additively manufactured using biocompatible materials such that the solid and porous aspects of the screw are fused together into a single construct. In yet another aspect, the fixation device comprises at least a portion or section incorporating a porous structure, which enables bony ingrowth through the porous section/portion of the screw, and thereby facilitates biocompatibility and improve mechanical characteristics. Methods for using the fixation device are also described herein.

A minimally invasive surgical procedure for replacing a hip joint is provided. A main incision is initiated at a point being a projection of a tip of a greater trochanter and extends proximally about a distance in the range of from 1 cm to 8 cm in line with the femoral axis. An inline capsulotomy is performed, while keeping muscles and posterior capsule intact, to expose the hip joint capsule for accessing the hip joint. The femoral canal is prepared for receipt of a femoral implant. The femoral head is resected and removed out of the acetabulum. A step of acetabular preparation is performed using a retractor comprising two tip rails, each tip rail having a plurality of tines. Related tools, devices, systems and methods are also provided.

A minimally invasive surgical procedure for replacing a hip joint is provided. A main incision is initiated at a point being a projection of a tip of a greater trochanter and extends proximally about a distance in the range of from 1 cm to 8 cm in line with the femoral axis. An inline capsulotomy is performed, while keeping muscles and posterior capsule intact, to expose the hip joint capsule for accessing the hip joint. The femoral canal is prepared for receipt of a femoral implant. The femoral head is resected and removed out of the acetabulum. A step of acetabular preparation is performed using a retractor comprising two tip rails, each tip rail having a plurality of tines. Related tools, devices, systems and methods are also provided.

A build plate includes a surface that defines at least one opening configured for disposal of a proximal portion of a screw shaft. The proximal portion is formed by a first manufacturing method and defines a distal face. The proximal portion is connected with the surface in a configuration to orient the distal face for forming a distal portion of the screw shaft thereon by a second manufacturing method that includes an additive manufacturing apparatus. In some embodiments, systems, spinal constructs, surgical instruments and methods are disclosed.

The present invention provides a prosthetic device including a pad-shaped spacer (100) including expandable layers (30) having a structure that expands in response to the introduction of moisture because the expandable layers (30) are made of a hydrogel material, so that in a surgery or treatment process, water is absorbed into the expandable layers (30) and fill a space inside a muscle or joint (J) tissue in a state in which the spacer (100) is implanted inside the space inside the muscle or joint (J) tissue until a new tissue grows inside the muscle or joint (J) tissue for a predetermined period of time, and the expandable layers (30) degrade gradually at a rate corresponding to a rate at which the tissue grows, with the result that the muscle or joint (J) tissue can be used during a recovery period.

A method and system for promoting the union of a bone fracture and/or fusion of bones across a joint space at a target region of a subject which may be accomplished by: inserting a surgical implant device at the target region; providing a guide member in the surgical implant device bore; sealing the surgical implant device bore distal opening and/or the surgical implant device bore proximal opening with the guide member; and positioning the guide member relative to the surgical implant device to provide for the guide member to be partially absent from the surgical implant device bore to allow the biomaterial and/or biologically active agents to extrude or diffuse from the activated apertures to the target region of the subject.

The present disclosure is directed to temporary antimicrobial-eluting cement spacer implants, and assemblies, kits, and methods for forming the same. Particularly preferred disclosures are to modular spacers, assemblies, and kits, as well as methods of manufacturing the same, where the modular nature of the spacer permits the selection of specific desired length spacers, as well as specific selection of antimicrobial compounds and dosages, along with the components and processes for forming the same.

The present disclosure relates to a gradually expanding limb reconstruction system (100) comprising at least one fixator mechanism (100a) and at least one distractor mechanism (100b) wherein distractor mechanism is a self-driven growing rod system (500) comprising at least one cylindrical static rod (502) with an internal bore; at least one piston rod (506), coaxially coupled with said static rod (502) and configured to distract longitudinally out of the static rod (502); at least one fluid receptacle component (508) in the internal bore of the static rod (502); at least one fluid source (510) configured to hold at least one sterile biocompatible fluid at a pre-determined pressure; at least one pressure and flow control unit (512) configured to release metered doses of the sterile biocompatible fluid from the fluid source (510) to the fluid receptacle component (508) via at least one fluid transfer port (514).

Various embodiments of wedge plates configured to promote bone growth are disclosed. Generally, a wedge plate comprises a first bone contact section, a second bone contact section, and a wedge section located between the first bone contact section and the second bone contact section. The wedge section is sized and configured to be received within a wedge formed in a bone. The wedge section comprises at least one feature configured to promote bone growth. A bone growth stimulant may be located within the at least one feature.