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FDA 510(k)

Arthrex MaxForce MTP Compression Plates and Screws

K-Number: K201235 · 2020-07-06

ApplicantArthrex, Inc.
Decision Date2020-07-06
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex MaxForce MTP Compression Plates and Screws is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2020-07-06 under approval number K201235. 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 MaxForce MTP Compression Plates and Screws?

Arthrex MaxForce MTP Compression Plates and Screws is a medical device that received FDA 510(k) clearance on 2020-07-06. It is manufactured by Arthrex, Inc.. The 510(k) number is K201235.

When was Arthrex MaxForce MTP Compression Plates and Screws approved by the FDA?

Arthrex MaxForce MTP Compression Plates and Screws received FDA 510(k) clearance on 2020-07-06, under approval number K201235.

What company makes Arthrex MaxForce MTP Compression Plates and Screws?

Arthrex MaxForce MTP Compression Plates and Screws is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex MaxForce MTP Compression Plates and Screws?

The FDA product code for Arthrex MaxForce MTP Compression Plates and 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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