MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE)

MOSS MIAMI SPINAL SYSTEM (ANTERIOR USE) is an FDA 510(k)-cleared medical device (K953915) manufactured by Depuy, 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 14, 1996. Regulation: 8.