VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS

VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS is an FDA 510(k)-cleared medical device (K120867) manufactured by Medos International SARL. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 2012. Regulation: 8.