← Product Code [SDZ](/productcode/SDZ) · P250033

# NEXUS Aortic Arch Stent Graft System (P250033)

_Endospan , Ltd. · SDZ · Apr 2, 2026 · APPR_

**Canonical URL:** https://fda.innolitics.com/device/P250033

## Device Facts

- **Applicant:** Endospan , Ltd.
- **Product Code:** [SDZ](/productcode/SDZ.md)
- **Decision Date:** Apr 2, 2026
- **Decision:** APPR
- **Device Class:** Class 3

## Regulatory Identification

Endovascular Repair of Ascending Aorta and Aortic Arch Lesions

---

**Source:** [https://fda.innolitics.com/device/P250033](https://fda.innolitics.com/device/P250033)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a PMA](https://innolitics.com/services/regulatory/), [a 510(k)](https://innolitics.com/services/510ks/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com