FDA 510(k), K172399, MicroMatrix

FDA 510(k), K172399, MicroMatrix

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510(K) Number: K172399
Device Name: MicroMatrix
Manufacturer: ACell, Inc.
Device Classification Name: wound dressing with animal-derived material(s)
Regulation Number:
Classification Product Code: KGN
Date Received: 08/08/2017
Decision Date: 10/06/2017
Regulation Medical Specialty:

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