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FDA 510(k) K153754, MicroMatrix, by Acell, Inc.

FDA 510(k) K153754, MicroMatrix, by Acell, Inc.

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510(K) Number: K153754
Device Name: MicroMatrix
Manufacturer: Acell, Inc.
Device Classification Name: wound dressing with animal-derived material(s)
Regulation Number:
Classification Product Code: KGN
Date Received: 12/29/2015
Decision Date: 03/14/2016

Total pages: 126
Fully redacted pages: 33
Content pages: 93

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