LigaMetrics Suture Anchors

LigaMetrics Suture Anchors is an FDA 510(k)-cleared medical device (K171964) manufactured by Mortise Medical, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2017. Regulation: 8.