Phoenix Wound Matrix— 510(k) K173544

Name: FDA 510(k) clearance K173544
Creator: U.S. Food and Drug Administration
Published: 2018-03-02

Substantially Equivalent

Nanofiber Solutions, Inc.

FDA 510(k) clearance K173544 for Phoenix Wound Matrix, Substantially Equivalent on 2018-03-02. Applicant: Nanofiber Solutions, Inc.. Device class: Unclassified.

Clearance details

Applicant: Nanofiber Solutions, Inc.
Product code: Code QSZ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2017-11-16
Decision date: 2018-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hilliard, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.