FDA 510(k)

Miromatrix Biological Mesh TW

K-Number: K162570 · 2017-02-16

Decision Date2017-02-16

Product CodeFTM

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Miromatrix Biological Mesh TW is a medical device manufactured by Miromatrix Medical, Inc.. It received FDA 510(k) clearance on 2017-02-16 under approval number K162570. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Miromatrix Biological Mesh TW?

Miromatrix Biological Mesh TW is a medical device that received FDA 510(k) clearance on 2017-02-16. It is manufactured by Miromatrix Medical, Inc.. The 510(k) number is K162570.

When was Miromatrix Biological Mesh TW approved by the FDA?

Miromatrix Biological Mesh TW received FDA 510(k) clearance on 2017-02-16, under approval number K162570.

What company makes Miromatrix Biological Mesh TW?

Miromatrix Biological Mesh TW is manufactured by Miromatrix Medical, Inc..

What is the FDA product code for Miromatrix Biological Mesh TW?

The FDA product code for Miromatrix Biological Mesh TW is FTM.

Other Devices by Miromatrix Medical, Inc.

K160400Miromatrix Biological Mesh

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.