KIRSCHNER BONE FIXATION FASTENER SYSTEM

KIRSCHNER BONE FIXATION FASTENER SYSTEM is an FDA 510(k)-cleared medical device (K854445) manufactured by Kirschner Medical Corp.. 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 18, 1985. Regulation: 8.