STEALTHSTATION TREATMENT GUIDANCE PLAFFORM

STEALTHSTATION TREATMENT GUIDANCE PLAFFORM is an FDA 510(k)-cleared medical device (K983397) manufactured by Surgical Navigation Technologies, 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 December 3, 1998. Regulation: 8.