NavLock Trackers, Robotic Reference Frame

NavLock Trackers, Robotic Reference Frame is an FDA 510(k)-cleared medical device (K182104) manufactured by Medtronic Navigation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 2018. Regulation: 8.