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Parker Quality & Compliance

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510(k) clearance

Arthrex Plates, Screws and Pins, and Washers

FDA 510(k) source

510(k) number
K263602
Applicant
Arthrex, Inc.
Decision date
Oct 29, 2026
Date received
Sep 30, 2026
Decision
Substantially Equivalent
Clearance type
Special
Product code
HRS
Device type
Plate, Fixation, Bone
Device class
Class II
Regulation
21 CFR 888.3030
Advisory committee
Orthopedic
Statement or summary
Summary
Third party
N
Location
Naples, FL, US