OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY

OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY is an FDA 510(k)-cleared medical device (K130498) manufactured by Bacterin International, Inc.. 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 30, 2013. Regulation: 8.