PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE is an FDA 510(k)-cleared medical device (K990131) 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 March 1, 1999. Regulation: 8.