PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP

PILLING WECK SURGICAL AORTIC SPOON-JAW CLAMP is an FDA 510(k)-cleared medical device (K992174) manufactured by Pilling Weck Surgical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 2000. Regulation: 8.