Stellarex 0.035 OTW Drug-Coated Angioplasty Balloon
FDA premarket approval P160049/S023 · decided 2024-05-22
Approval details
- PMA number
- P160049
- Supplement
- S023
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Stellarex 0.035 OTW Drug-Coated Angioplasty Balloon
- Generic name
- Drug-Eluting Peripheral Transluminal Angioplasty Catheter
- Applicant
- The Spectranetics Corp.
- Date received
- 2024-04-24
- Decision date
- 2024-05-22
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- ONU
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Fremont, CA
- Statement
- updates to the annual stability sampling plan
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