BIOACTIVE BONE GRAFT PUTTY

BIOACTIVE BONE GRAFT PUTTY is an FDA 510(k)-cleared medical device (K132071) manufactured by Biostructures, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 9, 2014. Regulation: 8.