MOTOR DRIVEN EXTIRPATION INSTRUMENTS

MOTOR DRIVEN EXTIRPATION INSTRUMENTS is an FDA 510(k)-cleared medical device (K904859) manufactured by Aesculap, 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 14, 1991. Regulation: 8.