510(k) K252807

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

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 12, 2026
Date Received
September 3, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plate, Fixation, Bone
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type