ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE

ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K874585) manufactured by Angiomed U.S., Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 1, 1987. Regulation: 8.