LINAC SCALPEL FLOORSTAND

LINAC SCALPEL FLOORSTAND is an FDA 510(k)-cleared medical device (K964517) 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 March 31, 1997. Regulation: 8.