Optilume Urethral Drug Coated Balloon Catheter
FDA premarket approval P210020/S010 · decided 2025-06-23
Approval details
- PMA number
- P210020
- Supplement
- S010
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Optilume Urethral Drug Coated Balloon Catheter
- Generic name
- Catheter, Balloon, Urethral, Drug-Coated
- Applicant
- Urotronic, Inc.
- Date received
- 2024-12-16
- Decision date
- 2025-06-23
- Days to decision
- 189 days
- Decision code
- APPR
- Product code
- QRH
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- approval for packaging the Optilume Urethral DCB with the Optilume Basic Urological Balloon Dilation Catheter and Atrion Medical QL inflation device into a kit, an additional site to package the proposed kit, and a labeling change to remove the vascular meta-analysis information from the Instruction for Use.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| Optilume® High Pressure Urological Balloon Dilation Catheter (K250910) | Urotronic, Inc. | 2025-05-22 |
| Optilume Basic Urological Balloon Dilation Catheter (K191061) | Urotronic, Inc. | 2020-01-02 |