C7 ANTERIOR CERVICAL INTERVERTEBRAL FUSION CAGE

C7 ANTERIOR CERVICAL INTERVERTEBRAL FUSION CAGE is an FDA 510(k)-cleared medical device (K121320) manufactured by Medyssey Co, Ltd.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 9, 2012. Regulation: 8.