ARTHTOTEK PRECISION HAND INSTRUMENTATION

ARTHTOTEK PRECISION HAND INSTRUMENTATION is an FDA 510(k)-cleared medical device (K933070) manufactured by Biomet, 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 March 23, 1994. Regulation: 8.