Spinecraft LLC

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Web: http://www.spinecraft.com
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Address: 2215 Entreprise Dr., Westchester, Illinois 60154, USA
Phone: +1-(708)-531-9700 | Fax: +1-(708)-531 9702 | Map/Directions >>

Profile: Spinecraft LLC develops and manufactures spine surgery implants & instrument systems & surgical tools. We provide comprehensive spine care solutions for patients with back pain, neck pain, degenerative disc conditions, spine deformities and disorders due to trauma. We offer products for cervical, thoracolumbar, interbody fusion, non-fusion applications & orthobiologics and bone substitutes. Our Apex deformity spine system is comprised of implants and instruments for stabilization of the spine during fusion in the thoracic, lumbar & sacral regions.

FDA Registration Number: 3004717358

14 Products/Services (Click for related suppliers)

• Anterior Cervical Plate

• 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.

• Cervical Intervertebral Fusion Device With Bone Graft (FDA Code: ODP / 888.3080)

• Deformity Spine Systems

• Intersomatic Lumbar Cages

• Low Back Spine Systems

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

• Osteoinduction Bone Void Filler (FDA Code: MBP / 888.3045)

• 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.

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

• Synthetic Bone Substitute

• Transforaminal Lumbar Cages