LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE

LISTING PODIATRY AS INTENDED USE FOR ENDOGUIDE is an FDA 510(k)-cleared medical device (K896711) manufactured by Luxar Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 1990. Regulation: 8.