DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM

DEPUY MOTECH TITANIUM MOSS MIAMI SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K964024) 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 March 25, 1997. Regulation: 8.