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FDA 510(k) Applications Submitted by ACell, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180776
03/23/2018
Cytal Wound Particulate
ACell, Inc.
K182259
08/21/2018
Gentrix Surgical Matrix, Gentrix Surgical Matrix Hiatal
ACell, Inc.
K191734
06/28/2019
MatriStem UBM Pericardial Patch
Acell, Inc.
K192725
09/27/2019
Cytal Wound Matrix 3-Layer
ACell, Inc.
K170763
03/13/2017
Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix Extend
ACell, Inc.
K172399
08/08/2017
MicroMatrix
ACell, Inc.
K162554
09/13/2016
Gentrix Surgical Matrix
Acell, Inc.
K230980
04/05/2023
MicroMatrix« Flex
ACell, Inc.
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