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FDA 510(k)

Arthrex Mesh Plate System

K-Number: K170547 · 2017-09-01

ApplicantArthrex, Inc.
Decision Date2017-09-01
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Mesh Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2017-09-01 under 510(k) number K170547. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Mesh Plate System?

Arthrex Mesh Plate System is a medical device that received FDA 510(k) clearance on 2017-09-01. The listed applicant is Arthrex, Inc.. The 510(k) number is K170547.

When did Arthrex Mesh Plate System receive FDA 510(k) clearance?

Arthrex Mesh Plate System received FDA 510(k) clearance on 2017-09-01, under 510(k) number K170547.

Who is the listed applicant for Arthrex Mesh 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 Mesh Plate System?

The FDA product code for Arthrex Mesh Plate System is HRS.

Other records listing Arthrex, Inc. as applicant

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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.

K260277MIKRON TRAUMA BONE PLATE& SCREW SYSTEMMikron Makina San. ve Tic. Ltd. Sti.K261511Xpert AnkleNewclip TechnicsK261406Versalock Proximal Tibial Plating SystemGM Dos Reis Industria e Comercio Ltda.K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB )TriMed, Inc.K261191Alians Elbow SNewclip TechnicsK261054RibPlate SystemStryker Leibinger GmbH & Co KG

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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