MEDYSSEY ANTERIOR CERVICAL FUSION CAGE

MEDYSSEY ANTERIOR CERVICAL FUSION CAGE is an FDA 510(k)-cleared medical device (K132732) manufactured by Medyssey USA, 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 July 17, 2014. Regulation: 8.