Duo Venous Stent System
FDA premarket approval P230021/S001 · decided 2025-02-11
Approval details
- PMA number
- P230021
- Supplement
- S001
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Duo Venous Stent System
- Generic name
- Stent, iliac vein
- Applicant
- Philips Image Guided Therapy Corporation
- Date received
- 2025-01-13
- Decision date
- 2025-02-11
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- QAN
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Plymouth, MN
- Statement
- a change to the Vesper Medical operating location
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| IntraSight Plus (K253714) | Philips Image Guided Therapy Corporation | 2026-02-24 |
| VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D) (K251103) | Philips Image Guided Therapy Corporation | 2025-05-09 |
| VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter (K200812) | Philips Image Guided Therapy Corporation | 2020-09-02 |
| Reconnaissance PV .018 OTW Digital IVUS Catheter (K200410) | Philips Image Guided Therapy Corporation | 2020-05-22 |