PTI STERNAL CLOSURE WIRE SUTURE

PTI STERNAL CLOSURE WIRE SUTURE is an FDA 510(k)-cleared medical device (K910067) manufactured by Pioneering Technologies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 5, 1991. Regulation: 8.