Responsive Arthroscopy Wedge Push-In Suture Anchors

Responsive Arthroscopy Wedge Push-In Suture Anchors is an FDA 510(k)-cleared medical device (K190446) manufactured by Responsive Arthroscopy, 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 March 26, 2019. Regulation: 8.