Arbor Endovascular, LLC
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories1
Latest Approval2026-03-19
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 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.