DAVOL ARTHRO-FLO 3

DAVOL ARTHRO-FLO 3 is an FDA 510(k)-cleared medical device (K951026) manufactured by Davol Inc., Sub. C. R. Bard, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 1, 1995. Regulation: 8.