INTERBODY INNOVATIONS CEMENT RESTRICTOR

INTERBODY INNOVATIONS CEMENT RESTRICTOR is an FDA 510(k)-cleared medical device (K051371) manufactured by Interbody Innovations, Llp. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 5, 2005. Regulation: 8.