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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 a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2017-09-01 under approval 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. It is manufactured by Arthrex, Inc.. The 510(k) number is K170547.

When was Arthrex Mesh Plate System approved by the FDA?

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

What company makes Arthrex Mesh Plate System?

Arthrex Mesh Plate System is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Mesh Plate System?

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

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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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