# P250033: NEXUS Aortic Arch Stent Graft System

- Pathway: PMA
- Applicant: Endospan, Ltd.
- Decided: Apr 2, 2026 after 223 days
- Product code: SDZ (Endovascular System For Treatment Of Ascending Aorta And Aortic Arch Lesions)
- Device class: 3
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P250033
Methodology: https://510kreport.com/methodology