Background

coflex™ is both an interspinous and interlaminar device that provides segmental stabilization; controlling motion rather than providing fusion. coflex™ is indicated for spinal stabilization after surgically addressing neural compression from soft and bony stenosis of the spinal cord.
The interlaminar stabilization provided by coflex™ is ideal for facet joint arthrosis and all related decompression procedures, as it offloads the facet joints.

coflex™ has more than 15 years of clinical data and over 32000 procedures have been carried out, which have proven the clinically successful concept of the implant.
 

Specific Indication

For patients who fail conservative treatment, but who are not candidates for a complete laminectomy or an irreversible procedure such as fusion, coflex™ may be the answer. The main indications are; radiographically confirmed moderate to serve stenosis with neural element compromise resulting in claudication and / or radicular symptoms isolated to 1 or 3 levels, in the region of L1 to L5 with or without concomitant low back pain.

coflex™ is more than a spacer – it is a functionally dynamic implant.