OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070

OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070 is an FDA 510(k)-cleared medical device (K133583) 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 February 9, 2014. Regulation: 8.