MODIFICATION TO BONE GRAFT SYRINGE

MODIFICATION TO BONE GRAFT SYRINGE is an FDA 510(k)-cleared medical device (K062173) manufactured by Wrightmedicaltechnologyinc. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 22, 2006. Regulation: 8.