Medtronic Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 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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