Superion Clinical Research
VertiFlex® has compiled the largest, most rigorous body of device clinical evidence related to relieving the pain of moderate lumbar spinal stenosis (LSS). 470 patients have been enrolled in a Superion U.S. IDE trial, as well as approximately 200 additional patients in 3 Superion studies outside the United States. The data from all studies suggest significant relief from the symptoms of spinal stenosis is achievable, along with very high patient satisfaction with the surgery.
Caution: Restricted by U.S. law to investigational use only© 2014 VertiFlex Inc.