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FDA 510(k)

Arthrex Compression Screws

K-Number: K201132 · 2020-07-27

ApplicantArthrex, Inc.
Decision Date2020-07-27
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Compression Screws is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2020-07-27 under approval number K201132. 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 Compression Screws?

Arthrex Compression Screws is a medical device that received FDA 510(k) clearance on 2020-07-27. It is manufactured by Arthrex, Inc.. The 510(k) number is K201132.

When was Arthrex Compression Screws approved by the FDA?

Arthrex Compression Screws received FDA 510(k) clearance on 2020-07-27, under approval number K201132.

What company makes Arthrex Compression Screws?

Arthrex Compression Screws is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Compression Screws?

The FDA product code for Arthrex Compression Screws 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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