COMPASS CT STEREOTACTIC ADAPTATION SYSTEM

COMPASS CT STEREOTACTIC ADAPTATION SYSTEM is an FDA 510(k)-cleared medical device (K862220) manufactured by Stereotactic Medical Systems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 1986. Regulation: 8.