SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)

SILASTIC BONE PLUG H.P.(CEMENT RESTRICT) is an FDA 510(k)-cleared medical device (K800898) manufactured by Dow Corning Corp. Healthcare Industries Materials. 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.