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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