SURGICAL INST.:1030,1010,1011,1012,1013,1014,1015

SURGICAL INST.:1030,1010,1011,1012,1013,1014,1015 is an FDA 510(k)-cleared medical device (K904479) manufactured by Percutaneous Technologies. 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 1, 1990. Regulation: 8.