Theken Spine

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Web: http://www.thekenspine.com
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Address: 1800 Triplett Blvd., Akron, Ohio 44306, USA
Phone: +1-(330)-475-8600 | Fax: +1-(330)-773-7697 | Map/Directions >>

Profile: Theken Spine designs, develops, manufacturers and distributes a full range of spinal fusion implants including cervical plates, pedicle screw systems, interbody systems, & trauma devices. Our Coral pedicle screw system is a fusion implant system used for the correction and stabilization of the lumbar or lower region of the spine. Our FormPutty is a beta-tricalcium phosphate putty used to fill bone voids. It is an osteoconductive material for solid bone growth.

The company was founded in 1998.

9 Products/Services (Click for related suppliers)

• Anterior Cervical Plating System

• Friction Head Screw Systems

• Occipito-Cervico-Thoracic Stabilization System

• Spinal Fixation Device

• Spinal Fixation Device Implant (FDA Code: JDN / 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 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)

• Spinal Vertebral Body Replacement Device (FDA Code: MQP / 888.3060)

• Thoracic Fixation Systems