PIONEER SILICOAT STERNAL CABLE

PIONEER SILICOAT STERNAL CABLE is an FDA 510(k)-cleared medical device (K993286) manufactured by Pioneer Surgical Technology. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 22, 1999. Regulation: 8.