DUPUY CEMENT RESTRICTOR TRIALS & INSTR.

DUPUY CEMENT RESTRICTOR TRIALS & INSTR. is an FDA 510(k)-cleared medical device (K800894) 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 May 1, 1980. Regulation: 8.