LABELING FOR MYO/WIRE II STERNOTOMY SUTURES

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES is an FDA 510(k)-cleared medical device (K932513) manufactured by Alto Development Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1994. Regulation: 8.