ARTHREX DISTAL RADIUS PLATE SYSTEM
K-Number: K131474 · 2013-07-03
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Device Summary
Frequently Asked Questions
What is the ARTHREX DISTAL RADIUS PLATE SYSTEM?
ARTHREX DISTAL RADIUS PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2013-07-03. The listed applicant is Arthrex, Inc.. The 510(k) number is K131474.
When did ARTHREX DISTAL RADIUS PLATE SYSTEM receive FDA 510(k) clearance?
ARTHREX DISTAL RADIUS PLATE SYSTEM received FDA 510(k) clearance on 2013-07-03, under 510(k) number K131474.
Who is the listed applicant for ARTHREX DISTAL RADIUS PLATE SYSTEM?
The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTHREX DISTAL RADIUS PLATE SYSTEM?
The FDA product code for ARTHREX DISTAL RADIUS PLATE SYSTEM is HRS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Arthrex, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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