LUKENS 2-0 BRAIDED SILK SUTURES

LUKENS 2-0 BRAIDED SILK SUTURES is an FDA 510(k)-cleared medical device (K922254) manufactured by Quinton, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 31, 1992. Regulation: 8.