ANSPACH SUTURE ANCHOR

ANSPACH SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K965069) manufactured by The Anspach Effort, 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 February 11, 1997. Regulation: 8.