INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE

INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K131540) manufactured by Vertebral Technologies, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 2013. Regulation: 8.