ACE/FISCHER PERCUTANEOUS HALF PINS

ACE/FISCHER PERCUTANEOUS HALF PINS is an FDA 510(k)-cleared medical device (K875012) manufactured by Buckman Co., Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 1988. Regulation: 8.