Osteophilic Finish Uncemented Semi- Hip Prosthesis Suppliers
www.biomet.com/orthopedics | Send Inquiry | Phone: +1-(574)-267-6639
FDA Registration: 1825034 Year Established: 1977 Annual Revenues: > USD 1 Billion Employee Count: ~20 Quality: ISO 9001, CE Certified
Products: Drills, Drills Accessories, High Speed Orthopedic Drills, Surgical Drills, Orbital Procedures, Bone Drills, Orthopedics, High Speed Drills System, ...
Biomet, Inc designs and manufactures products for hip replacement, knee replacement, shoulder replacement, elbow replacement & other small joint replacements. We are an ISO 9001 CE certified company. more...
www.wmt.com | Send Inquiry | Phone: +1-(901)-867-9971, 800-238-7117
FDA Registration: 3012429289 Year Established: 1950 Annual Revenues: USD 100-500 Million Employee Count: ~1000 Quality: ISO 9002, ISO 9003, CE Certified
Products: Tibial Inserts, Patellar Implants, Metal and Ceramic Liners, All Poly Liners, Femoral Components, Total Shoulder Systems, ...
Wright Medical Technology, Inc. is a global orthopaedic medical device company. Our Advance® Uni-Knee renders normal motion and leads to a longer implant life that delays or prevents the need for more...
www.chattgroup.com | Phone: +1-(423)-870.2281, 800.592.7329
Year Established: 1947 Annual Revenues: USD 50-100 Million Employee Count: ~300 Quality: ISO 9001, CE Certified
Products: Carts, Chairs & stools, Compression Garments, Cryosurgery, EKG Supplies, Exam Tables, ...
Chattanooga Group produces rehabilitation equipment for treating skeletal, muscular, neurological and soft tissue disorders. Our laser therapy uses light to penetrate tissue for increased blood flow a more...
www.djosurgical.com | Phone: +1-(512)-832-9500, 800-456-8696
FDA Registration: 1644408
Products: Drill Bit (FDA Code: HTW), Nail Extractors (FDA Code: HWB), AC-Powered Motor Orthopedic Surgical Instrument (FDA Code: HWE), Orthopedic Burr (FDA Code: HTT), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Prosthesis Driver (FDA Code: HWR), ...
Encore Medical, L.P. is a designer, manufacturer and distributor of orthopedic surgery products. Our Reverse® shoulder prosthesis is indicated for use in patients with a functional deltoid muscle, more...
Phone: 972-9-951151
FDA Registration: 9615128
Products: AC-Powered Surgical Instrument Motor (FDA Code: GEY), Bone Fixation Nail (FDA Code: JDS), Intramedullary Fixation Rod and Accessories (FDA Code: HSB), Metal/Polymer Femoral Hemi- Hip Prosthesis (FDA Code: KWY), Uncemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LWJ), Cemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: JDI), ...
Disc-O-Tech Medical Technologies, Ltd. are providers of battery powered screwdrivers and intramedullary fixation rods. more...
Phone: +49-(7)-462-2080
FDA Registration: 8010764
Products: Flexible Depth Gauge (FDA Code: HTJ), Bone Fixation Screw (FDA Code: HWC), Intramedullary Fixation Rod and Accessories (FDA Code: HSB), Invasive Traction Component (FDA Code: JEC), Orthopedic Manual Surgical Instrument (FDA Code: LXH), Proximal Femoral Fixation Implant Device (FDA Code: JDO), ...
Smith & Nephew Orthopaedics, Gmbh offers bone fixation screws, cement obturators, acetabular mesh hip prosthesis and orthopedic stereotaxic instruments. more...
A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.
Classification. Class II.
