INTERPORE CROSS CEMENT RESTRICTOR

INTERPORE CROSS CEMENT RESTRICTOR is an FDA 510(k)-cleared medical device (K032095) manufactured by Interpore Cross Intl.. 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 August 7, 2003. Regulation: 8.