Profile: Global Orthopaedic Technology, Pty, Llc offers products and services within the orthopedic & neuro-surgical industries. Our products include Edinburgh cemented hip system, Apex Modular™ hip system, Bio-ball® system, SMR revision hip system, SuperCable™, RBK Patello-Femoral resurfacing system , GRU™ knee and Actifuse™. Our SuperCable™ features fatigue strength superior to both wire and cables thereby reducing complications due to breakage. It provides long-term dynamic compressive loading across bone fragments to offer the possibility for better healing and increased strength. It can be easily re-tightened to adjust cable tension, especially when multiple cables are applied, both saving time and reducing the number of cables required. Our C~ment is a product range of bone cements that are used for the fixation of artificial joints. Bone cement fills the space between the prosthesis and the bone. It allows for an immediate and stable fixation of the surgical implant.
2 Products/Services (Click for related suppliers)
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| • Semi-Constrained Femorotibial Knee Prosthesis (FDA Code: HRY / 888.3530) A knee joint femorotibial metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee 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 includes prostheses that consist of a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027). |
| • Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR / 888.3540) A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. 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 includes a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component. |