Lutonix 018 Drug Coated Balloon Catheter
FDA premarket approval P170003/S023 · decided 2021-08-05
Approval details
- PMA number
- P170003
- Supplement
- S023
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Lutonix 018 Drug Coated Balloon Catheter
- Generic name
- Drug-coated peripheral transluminal angioplasty catheter
- Applicant
- Lutonix
- Date received
- 2021-07-06
- Decision date
- 2021-08-05
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- PRC
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- New Hope, MN
- Statement
- Replacement of a manual feed system with an automated feed system.
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