CONMED LINVATEC OSPREY DRILL SYSTEM

CONMED LINVATEC OSPREY DRILL SYSTEM is an FDA 510(k)-cleared medical device (K080444) manufactured by Conmed Linvatec. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 1, 2008. Regulation: 8.