CODMAN COLLINS RADIOPARENT STERNAL BLADES

CODMAN COLLINS RADIOPARENT STERNAL BLADES is an FDA 510(k)-cleared medical device (K904352) manufactured by Codman & Shurtleff, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 20, 1990. Regulation: 8.