VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE

VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE is an FDA 510(k)-cleared medical device (K991706) manufactured by Stryker Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 1999. Regulation: 8.