For decades, the surgical options for patients with lumbar spinal stenosis (LSS) were limited to either decompression or decompression with spinal fusion. In 2012, the FDA approved the coflex® Interlaminar Stabilization device, a small U-shaped titanium implant that provides spinal stability, with maintenance of motion and segmental stabilization.

The coflex® implant in Action

After surgical decompression, which removes pressure on the impinged nerves, your spine surgeon will insert the coflex® implant through the same small incision. The device is positioned on the lamina, which is the strongest bone in the back of your spine.

The design of the coflex® implant maintains stability in the spine, while preserving motion at the treated level. If you suffer from leg and/or back pain caused by spinal stenosis you could be a candidate for the coflex® implant.

The benefits of the coflex® implant when compared to pedicle screws fusion include:

  • Faster relief of symptom

  • Quicker recovery

  • Less time in the OR

  • Shorter hospital stay

  • More satisfied with outcome

Additionally, for qualified people, the coflex® procedure can be performed in an outpatient setting which can contribute to better outcomes, lowered infection rates, decreased medical costs, and a higher quality experience overall.1 For more information about the coflex® implant download our coflex® implant Education Brochure.

*Every patient is different; therefore, results may vary.

¹Sector Report: Ambulatory Surgery Centers (ASCs) in a time of COVID-19- Healthcare Sector Spotlight Q2 2020- FocalPoint Investment Banking, May 2020.

https://focalpointllc.com/wp-content/uploads/2020/05/Ambulatory-Surgery-Centers-Spotlight.pdf 

When you’re ready to begin, contact our team and speak with one of our patient support specialists. They can help guide you through the process and answer any questions about your treatment options.