Phoenix Wound Matrix
K-Number: K173544 · 2018-03-02
Device Summary
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. The listed applicant is Nanofiber Solutions, Inc.. The 510(k) number is K173544.
When did Phoenix Wound Matrix receive FDA 510(k) clearance?
Phoenix Wound Matrix received FDA 510(k) clearance on 2018-03-02, under 510(k) number K173544.
Who is the listed applicant for Phoenix Wound Matrix?
The FDA 510(k) record lists Nanofiber Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Phoenix Wound Matrix?
The FDA product code for Phoenix Wound Matrix is QSZ.
Other records listing Nanofiber Solutions, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QSZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.