GRAFT, MICROVEL GUIDELINE, STERILE

GRAFT, MICROVEL GUIDELINE, STERILE is an FDA 510(k)-cleared medical device (K760091) manufactured by Meadox Medicals, Div. Boston Scientific Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 1976. Regulation: 8.