TRITON ELECTRIC HIGH TORQUE HANDPIECE AND SOFTWARE MODULE

TRITON ELECTRIC HIGH TORQUE HANDPIECE AND SOFTWARE MODULE is an FDA 510(k)-cleared medical device (K121264) manufactured by Medtronic Surgical Technologies. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 2012. Regulation: 8.