LACTOSORB SUTURE ANCHOR

LACTOSORB SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K954443) manufactured by Poly-Medics,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 January 30, 1996. Regulation: 8.