Jupiter Endovascular
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Vertex™ Thrombectomy System (K261523) | Jupiter Endovascular | 2026-08-04 |
| Vertex(TM) Catheter (K252027) | Jupiter Endovascular | 2025-09-12 |
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