Arbor Endovascular, LLC
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories1
Latest FDA decision2026-08-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262424 | Willow 12 Guidewire | MOF | 2026-08-14 | View |
| 510(k) | K260537 | Willow 24 Guidewire | MOF | 2026-03-19 | View |
| 510(k) | K260130 | Willow 18 Guidewire | MOF | 2026-02-13 | View |
| 510(k) | K253168 | 0.014” Willow Guidewire | MOF | 2025-11-26 | View |
| 510(k) | K243756 | 0.014” Willow Guidewire | MOF | 2025-07-17 | View |
No matching devices.