Acell, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
Total Devices11
Categories3
Latest Approval2024-07-11
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K241724 | Cytal® Wound Matrix; Cytal® Burn Matrix | KGN | 2024-07-11 | View |
| 510(k) | K241706 | MicroMatrix® UBM Particulate | KGN | 2024-07-11 | View |
| 510(k) | K230980 | MicroMatrix® Flex | KGN | 2023-09-22 | View |
| 510(k) | K191734 | MatriStem UBM Pericardial Patch | PSQ | 2019-11-22 | View |
| 510(k) | K192725 | Cytal Wound Matrix 3-Layer | KGN | 2019-10-25 | View |
| 510(k) | K182259 | Gentrix Surgical Matrix, Gentrix Surgical Matrix Hiatal | FTM | 2019-02-07 | View |
| 510(k) | K180776 | Cytal Wound Particulate | KGN | 2018-05-11 | View |
| 510(k) | K172399 | MicroMatrix | KGN | 2017-10-06 | View |
| 510(k) | K170763 | Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix Extend | FTM | 2017-06-08 | View |
| 510(k) | K162554 | Gentrix Surgical Matrix | FTM | 2016-10-21 | View |
| 510(k) | K153754 | MicroMatrix | KGN | 2016-03-14 | View |
No matching devices.