K-CAP-I ORTHOPEDIC FIXATION WIRE CAP

K-CAP-I ORTHOPEDIC FIXATION WIRE CAP is an FDA 510(k)-cleared medical device (K902053) manufactured by Westcon Orthopedics, 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 September 13, 1990. Regulation: 8.