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FDA 510(k)

Phoenix Wound Matrix

K-Number: K173544 · 2018-03-02

ApplicantNanofiber Solutions, Inc.
Decision Date2018-03-02
Product CodeQSZ
DecisionSubstantially Equivalent

Device Summary

Phoenix Wound Matrix is a medical device manufactured by Nanofiber Solutions, Inc.. It received FDA 510(k) clearance on 2018-03-02 under approval number K173544. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Phoenix Wound Matrix?

Phoenix Wound Matrix is a medical device that received FDA 510(k) clearance on 2018-03-02. It is manufactured by Nanofiber Solutions, Inc.. The 510(k) number is K173544.

When was Phoenix Wound Matrix approved by the FDA?

Phoenix Wound Matrix received FDA 510(k) clearance on 2018-03-02, under approval number K173544.

What company makes Phoenix Wound Matrix?

Phoenix Wound Matrix is manufactured by Nanofiber Solutions, Inc..

What is the FDA product code for Phoenix Wound Matrix?

The FDA product code for Phoenix Wound Matrix is QSZ.

Related Clinical Trials

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Related Devices (Code: QSZ)

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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.

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