ANSPACH SUTURE ANCHOR (MODIFIED)

ANSPACH SUTURE ANCHOR (MODIFIED) is an FDA 510(k)-cleared medical device (K963686) 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 November 24, 1996. Regulation: 8.