Allez Spine, LLC

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Web: http://www.allezspine.com
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Address: 2301 Dupont Drive, Suite 510, Irvine, California 92612, USA
Phone: +1-(949)-752-7885, 800-939-7008 | Fax: +1-(949)-752-7886 | Map/Directions >>

Profile: Allez Spine, LLC designs, manufactures and distributes spinal fusion systems. We produce prototype products and customized instrumentation to meet the needs of spine surgeons. We provide Laguna® polyaxial pedicle screw system. Its screws are color coded by size and are available in a variety of lengths. Its features such as increased pull-out strength, improved access & graft visibility, & simplified instrumentation offer flexibility & choice to the surgeon. We also produce and distribute spinal implants.

FDA Registration Number: 3005032381

6 Products/Services (Click for related suppliers)

• 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 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.

• Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB / 888.3070)

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