510(k) K252807

Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates by Arthrex, Inc. — Product Code HRS

K252807 is an FDA 510(k) premarket notification submitted by Arthrex, Inc. for the device "Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates". The FDA issued a decision of Substantially Equivalent on January 12, 2026. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Arthrex, Inc. has at least 10 other 510(k) clearances on record.