NuDel Delivery System
FDA premarket approval P150028/S002 · decided 2018-11-14
Approval details
- PMA number
- P150028
- Supplement
- S002
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- NuDel Delivery System
- Generic name
- Aortic stent
- Applicant
- NuMED, Inc.
- Date received
- 2018-03-07
- Decision date
- 2018-11-14
- Days to decision
- 252 days
- Decision code
- APPR
- Product code
- PNF
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Hopkinton, NY
- Statement
- Approval for the NuDEL Delivery System.
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.
510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| BIB Stent Placement Catheter (K213915) | NuMED, Inc. | 2022-01-12 |
| Z-6 Atrioseptostomy Catheter (K211910) | NuMED, Inc. | 2021-07-19 |
| BIB Stent Placement Catheter (K211134) | NuMED, Inc. | 2021-05-27 |
| D'Vill Introducer (K190974) | NuMED, Inc. | 2019-05-14 |
| D'Vill Introducer (K171206) | NuMED, Inc. | 2017-10-20 |
| BIB Stent Placement Catheter (K161451) | NuMED, Inc. | 2016-09-22 |
| REBOA Balloon Catheter (K160598) | NuMED, Inc. | 2016-06-20 |
| BIB Stent Placement Catheter (K160889) | NuMED, Inc. | 2016-05-20 |