ROWE SHOULDER INSTR. FOR BANKHART REPAIR

ROWE SHOULDER INSTR. FOR BANKHART REPAIR is an FDA 510(k)-cleared medical device (K820344) manufactured by New England Surgical Instrument 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 7, 1982. Regulation: 8.