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A Spine USA Inc

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Web: http://www.aspine.net
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Address: 457 Mariposa St, San Francisco, California 94107, USA
Phone: +1-(415)-556-8888 | Map/Directions >>
 
 

Profile: A Spine USA specializes in orthopedic implant products for human spinal disease treatment. Our products are designed to relieve pain and minimize hospitalization. Our product line includes window system, trifix system and plate system. Our narrow plate system provides anterior stabilization and fixation for unstable thoracic vertebrae. Our product features include low profile, top-loading and thin. Our window system is dynamic and allows the settling of bone graft. We also offer cervi-link system that is designed to stabilize the cervical region from the occiput to T3.We also offer Vesselplasty. It is a new technique advancing the Kyphoplasty technique. It uses a PET artificial vessel, the vessel-X®, to restore the height of the vertebral body, it serving as a vertebral body expander and also serving as the bone void material container. It is introduced into the vertebra in a reduced configuration and once positioned within the vertebra, it is expanded to its predetermined configuration raising the endplates and creating a void along with the introduced of bone void filler material. And then, a few bone void filler material penetrates through vessel-X®, interdigitating the vertebral body. In the end, vessel-X® and the bone void filler material will be remained at the predetermined injected area.

14 Products/Services (Click for related suppliers)  
• Biomedical Devices
• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)
A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.
• General Surgical Instruments
• Spinal Anterior Narrow Plate System
• Spinal Anterior Straight Plate System
• 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 Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060)
A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.
• 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.
• Spine Supports
• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)
• Surgical Instrument (Miscellaneous Medical)
• Vertebral Disc Spacer System
• Vertebroplasty
• Vertebroplasty Implants

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