DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K980447) manufactured by DePuy Orthopaedics, 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 April 13, 1998. Regulation: 8.