coflex® in the News

The coflex® Interlaminar Stabilization® device has been widely adopted across the United States since its FDA approval in 2012. Check out these quick links and get a glimpse of the coflex® device and its media coverage from not only when it was under investigational study by the FDA, but also since its approval.




This product has since been FDA approved for use in the United States.


The views and opinions expressed on the sites and pages linked above are those of the individuals expressing them only, and are not intended to imply any affiliation with, or endorsement or recommendation of or by Paradigm Spine, LLC.