ACROMED WALLIE-HEINIG OSTEOTOMES

ACROMED WALLIE-HEINIG OSTEOTOMES is an FDA 510(k)-cleared medical device (K870780) manufactured by Buckman Co., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 1987. Regulation: 8.