Profile: Nutek® Orthopaedics develops and markets orthopaedic devices. Our orthopaedic devices include periarticular fixation devices and bone augmentations earmarked to preserve joint motion after the repair of devastating musculoskeletal injuries. Our product includes NBX® fixator. Our device is made of space-age, high strength polymers, assuring fracture stability, easy tolerance by the patient and unrestricted cleaning during normal bathing activities. The body of the fixator locks a matrix of multi-planar placed pins and keeps the device above the skin. The fracture complex is pinned and stabilized in anatomic position, proximal to the wrist joint only, thus allowing full and immediate range of motion. There is no dissection and fixation is based on percutaneous placement of small diameter pins.
FDA Registration Number: 3005893246
6 Products/Services (Click for related suppliers)
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• Cannulated Screw Fracture Fixation System |
• Multiple Component Fixation Appliance (FDA Code: KTT / 888.3030) Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system. |
• Nail/Blade/Plate Component Fixation Appliance (FDA Code: LXT / 888.3030) |
• Shoulder Fixators |
• Wrist Fixator |
• Wrist Reduction Devices |