Product code SDZ
- Device name
- Endovascular System For Treatment Of Ascending Aorta And Aortic Arch Lesions
- Medical specialty
- Unknown
- Device class
- 3
- Review panel
- CV
- Implant
- Y
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Definition
- Endovascular Repair of Ascending Aorta and Aortic Arch Lesions
- Source
- FDA openFDA device classification dataset
Related PMA Records
| PMA | Device | Applicant | Decision date |
|---|
| P250033S001 | NEXUS® Aortic Arch Stent Graft System | Endospan , Ltd. | 2026-05-20 |
| P250033 | NEXUS Aortic Arch Stent Graft System | Endospan , Ltd. | 2026-04-02 |
| P210032S015 | GORE TAG Thoracic Branch Endoprosthesis (TBE Device) | W. L. Gore & Associates, Inc. | 2025-04-11 |