Patients Like You in the FDA Study

Patient Success Comparator

In the clinical study, patients with moderate to severe spinal stenosis either received a coflex® device or the current standard of care, pedicle screw fusion, to relieve their back pain. If you have been diagnosed with moderate to severe spinal stenosis, please complete the form to see how pain was relieved for patients like you.
 lbs (e.g., 175)
 years old (e.g., 42)
Disclaimer: Although the coflex® device provides tremendous benefits to many patients, it is not for everyone. The data used in this patient comparator is based on a randomized FDA clinical study comparing the coflex® Interlaminar Technology to the standard of care, pedicle screw fusion surgery. The study consisted of 322 randomized patients (215 coflex®; 107 fusion) at 21 clinical centers. Successful pain relief was measured by a 15-point improvement in Oswestry Low Back Pain Disability Index (ODI). This content is for educational purposes only and does not replace having a conversation with your doctor.