LINAC SCALPEL TREATMENT PLANNING SYSTEM

LINAC SCALPEL TREATMENT PLANNING SYSTEM is an FDA 510(k)-cleared medical device (K962792) manufactured by Surgical Navigation Technologies, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 11, 1996. Regulation: 8.