Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates

Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates is an FDA 510(k)-cleared medical device (K252807) 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 January 11, 2026. Regulation: 8.