Elite Surgical Supplies (pty) Ltd

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Contact: Rudi Verbeek
Web: http://www.elitesurgical.com
E-Mail:
Address: 184 Bessemer Rd, Pretoria West, Pretoria 0183, South Africa
Phone: +27-(12)-3860012 | Fax: +27-(12)-3862745 | Map/Directions >>

Profile: Elite Surgical Supplies (pty) Ltd is engaged in the business of arthroplasty and orthopaedic devices. Our arthoplasty products include bone cements, hips, knee, and shoulders. Our spinal product line comprises of cervical plating systems, intervertebral cages and pedicle screws. Narrow D.C. plates are used for achieving osteosynthesis in fractures of the tibia, radius, ulna and pelvis. Collafoam is used to treat neck strains and sprains by restricting movement of the cervical vertebrae and supporting the head. It is typically used for neck injuries requiring longer-term treatment. It is secured in place by means of two tubular bandage straps with a built-in touch-and-close Velcro fastener. The Elite modular total shoulder is a total joint replacement prosthesis ideally suited for a cemented, total or partial joint arthroplasty. Small-fragment plates are used for the treatment of fractures of the malleoli, fibula, distal radius, and elbow, as well as for the fixation of small fragments in large bones. It is also used in conjunction with 3.5mm screws.

FDA Registration Number: 3005325790
US Agent: Steve Baker / I-smart Consulting Us
Phone: +1-(267)-432-1045 E-Mail:

10 Products/Services (Click for related suppliers)

• Bone Cement (FDA Code: LOD / 888.3027)

Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.

• Bone Fixation Plate (FDA Code: HRS / 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.

• Bone Fixation Screw (FDA Code: HWC / 888.3040)

A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Bone Screws

• Cervical Collars

• Pedicle Screws

• Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 888.3050)

A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome.

• Spinal Pedicle Fixation Orthosis (FDA Code: MNI / 888.3070)

Pedicle screw spinal systems are multiple component devices, made from a variety of materials, including alloys such as 316L stainless steel, 316LVM stainless steel, 22Cr-13Ni-5Mn stainless steel, Ti-6Al-4V, and unalloyed titanium, that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. Such a spinal implant assembly consists of a combination of anchors (e.g., bolts, hooks, and/or screws); interconnection mechanisms incorporating nuts, screws, sleeves, or bolts; longitudinal members (e.g., plates, rods, and/or plate/rod combinations); and/or transverse connectors.

• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)

• Steinman Pins