510(k) K263602

Device
Arthrex Plates, Screws and Pins, and Washers
Applicant
Arthrex, Inc.
510(k) number
K263602
Product code
HRS
Decision
Substantially Equivalent (SESE)
Decision date
2026-10-29
Date received
2026-09-30
Regulation
888.3030
Classification name
Plate, Fixation, Bone
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Rebecca Homan
Address
1370 Creekside Blvd. Naples FL US 34108 34108

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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