ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR

ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K925328) manufactured by Anspach Mfg., 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 October 26, 1993. Regulation: 8.