Life Spine

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Contact: Michael Butler
Web: http://www.lifespine.com
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Address: 2401 W. Hassell Rd., Suite 1535, Hoffman Estates, Illinois 60169, USA
Phone: +1-(847)-8846117 | Fax: +1-(847)-8846118 | Map/Directions >>

Profile: Life Spine is a developer, manufacturer and marketer of proprietary medical devices serving the orthopedic and neurosurgery communities. Our cervical products include Neo, Neo-sl, Kinetic and Kinetic-sl. Our Neo system allows for generous screw angulation while providing a large graft window.The Neo-SL system is an ultra slim anterior cervical plating system with an integrated lock that allows bone screws to be securely fixed without any additional locking components. Our thoracolumbar products are Conquest, Lynx, Pilot and Plateau. Our Pilot spinal system delivers implants quickly while maximizing versatility and our Conquest poly axial screw system is available in both straight and arched versions in various lengths.

FDA Registration Number: 3004499989

15 Products/Services (Click for related suppliers)

• Anterior Cervical Plating System

• Cannulated Pedicle Screws

• Cement Restrictor Hip Prosthesis (FDA Code: JDK / 878.3300)

Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.

• Facet Screw Spinal Device System (FDA Code: MRW)

• Giardia Spp. (FDA Code: MHI / 866.3220)

• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080)

• Lumbar Solid-Sphere Intervertebral Fusion Device With Bone Graft (FDA Code: NVR)

• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)

An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

• Polyaxial Pedicular Screw 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.

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

• Spinal Systems

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