FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Arthrex Beaming System

K Number: K254215 · Decision May 8, 2026
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
348
Review Days
130

Basic Information

Device Name
Arthrex Beaming System
K Number
K254215
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
December 29, 2025
Decision Date
May 8, 2026
Product Code
HWC
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HWC Screw, Fixation, Bone

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K260353 Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
K254229 Arthrex Nano FiberTak Suture Anchor
K253713 Arthrex Variable Angle (VA) Proximal Tibia Plating System
K252807 Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
K253895 Arthrex SwiveLock Suture Anchor, 3.5 x 10 mm
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