Abre Venous Self-expanding Stent System
FDA premarket approval P200026/S009 · decided 2024-05-31
Approval details
- PMA number
- P200026
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Abre Venous Self-expanding Stent System
- Generic name
- Stent, iliac vein
- Applicant
- Medtronic Vascular, Inc.
- Date received
- 2024-05-29
- Decision date
- 2024-05-31
- Days to decision
- 2 days
- Decision code
- OK30
- Product code
- QAN
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Plymouth, MN
- Statement
- removal of two post-electropolishing visual inspection scrap codes at the Medtronic Nathan Lane manufacturing facility in Plymouth, Minnesota
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| Heli-FX EndoAnchor System (K182957) | Medtronic Vascular, Inc. | 2018-11-21 |
| Sentrant Introducer Sheath with Hydrophilic Coating (K171866) | Medtronic Vascular, Inc. | 2017-12-20 |
| SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System (K170191) | Medtronic Vascular, Inc. | 2017-06-16 |
| Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette (K171427) | Medtronic Vascular, Inc. | 2017-06-13 |
| HawkOne Directional Atherectomy System (K161361) | Medtronic Vascular, Inc. | 2016-10-14 |