Patients who suffer from spinal stenosis syndrome indicated on one or two levels are ideal candidates for interspinous implants. After conservative methods of treatment fail, the treating of these patients is continued surgically.

Interspinous implant overcomes the therapeutic gap between conservative and aggressive surgical methods of treatment and enables remission of patients discomfort along with minimal surgical risks.

Main indications for coflex interspinous implant are: radiographically confirmed moderate to severe stenosis of the spinal canal with clinical signs of neurogenic claudication and/or foraminal  stenosis syndrome caused by a degenerative process on the spine. Coflex implant is indicated to 1 or 2 levels in the region of L1 to S1.

Paradigm Spine Coflex Implant

Non-fusion procedures will allow for the spine to stabilize and restore its natural anatomical function and in some cases will lead to reduction of unnatural movements and healing of the damaged disk.

The procedure of inserting a coflex implant is a minimally invasive procedure that takes less than an hour and does not require a general anesthesia.