Medtronic Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
Total Devices11
Categories9
Latest FDA decision2026-07-10
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P110023 | STENT, SUPERFICIAL FEMORAL ARTERY | NIP | 2026-07-10 | View |
| PMA | P060001 | Stent, carotid | NIM | 2026-07-10 | View |
| PMA | P190008 | Drug-coated peripheral transluminal angioplasty catheter | PRC | 2026-05-21 | View |
| PMA | P200026 | Stent, iliac vein | QAN | 2026-04-27 | View |
| PMA | P140018 | Agent, occluding, vascular, permanent | PJQ | 2026-04-17 | View |
| PMA | P030045 | STENT, ILIAC | NIO | 2024-07-26 | View |
| 510(k) | K182957 | Heli-FX EndoAnchor System | OTD | 2018-11-21 | View |
| 510(k) | K171866 | Sentrant Introducer Sheath with Hydrophilic Coating | DYB | 2017-12-20 | View |
| 510(k) | K170191 | SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System | MCW | 2017-06-16 | View |
| 510(k) | K171427 | Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette | OTD | 2017-06-13 | View |
| 510(k) | K161361 | HawkOne Directional Atherectomy System | MCW | 2016-10-14 | View |
No matching devices.
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