OSTEOPLAST, MODEL POP200

OSTEOPLAST, MODEL POP200 is an FDA 510(k)-cleared medical device (K991854) manufactured by Interpore Cross Intl.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 25, 1999. Regulation: 8.