Made of PEEK-OPTIMA, the Idys™-C cage has been designed by a team with extensive experience in the development of spinal instrumentation. The design team focused on creating a cervical cage adapted to the vertebral anatomy in order to maintain disc height, restore cervical lordosis and stabilize the treated segment. Thus Idys™-C creating favorable conditions to optimize bone fusion.
Indications for use
The Idys™ C device is indicated for cervical interbody fusion procedures in
skeletally mature patients with cervical disc disease at one level from the C2-C3
disc to the C7-T1 disc. Cervical disc disease is defined as intractable radiculopathy and/or myelopathy with herniated disc and/or osteophyte formation on posterior vertebral endplates producing symptomatic nerve root and/or spinal
cord compression confirmed by radiographic studies. This device is to be used in
patients who have had six weeks of non-operative treatment. The Idys™ C device
is to be used with supplemental fixation. The Idys™ C device is also required to be used with autologous graft and is to be implanted via an open, anterior approach.
Federal law (USA) restricts this device to sale by or on the order of a physician. Prior to using any Clariance device, please review the instructions for use and surgical technique for a complete listing of indications, contraindications, warnings, precautions, potential adverse events, and directions for use.