Arthrex Spine Endoscope

Arthrex Spine Endoscope is an FDA 510(k)-cleared medical device (K243602) manufactured by Arthrex, 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 May 15, 2025. Regulation: 8.