ARTHROSCOPY SUCTION BIOPSY PUNCH

ARTHROSCOPY SUCTION BIOPSY PUNCH is an FDA 510(k)-cleared medical device (K850527) manufactured by T. Korossurgical Instruments Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 13, 1985. Regulation: 8.