OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE

OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K140716) manufactured by Interventional Spine, 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 November 23, 2014. Regulation: 8.