Arthrex VAL and VAL KreuLock™ Compression Screw System

Arthrex VAL and VAL KreuLock™ Compression Screw System is an FDA 510(k)-cleared medical device (K242554) 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 October 20, 2024. Regulation: 8.