A step forward in dynamic stabilization:
the coflex^® investigational implant

Paradigm Spine, LLC, is dedicated to providing non-fusion spinal implant solutions that address the unmet clinical needs of spine surgeons and their patients.

This commitment led to the development of the coflex Interspinous Stabilization Device, an interspinous process functional dynamic implant designed to create a stabilizing effect at the treated level(s).

The device consists of a single, U-shaped component made of medical-grade titanium alloy (Ti6A14V). In clinical use, the U is positioned horizontally, with its apex oriented anteriorly and the two long arms of the U paralleling the long axis of the spinous processes. The bone-facing surfaces are ridged to resist migration.

Implantation of the coflex device requires minimal extension of decompression surgery, and can usually be performed in 15 minutes or less following the decompression portion of the procedure.

The coflex spine study is currently underway to assess the safety and efficacy of the coflex device as compared to pedicle screw fixation and spinal fusion.

For more information on the coflex clinical research study, or to see if you might be eligible to participate, call 1-866-493-9510 Mon–Thurs, 7am– 7pm and Fri, 7am– 6pm, CST.

CAUTION: Investigational device. Limited by Federal (or United States) law to investigational use.