
C.R. Bard, Inc.
Free shipping on orders over $99 · 30-day returns
BARD VENTRALEX HERNIA PATCH, MODELS 0010302, 0010301 is an FDA 510(k)-cleared medical device (K021736) manufactured by C.R. Bard, Inc.. 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 July 15, 2002. Regulation: 8.