IntellaNav MiFi XP Ablation Catheter
FDA premarket approval P020025/S144 · decided 2025-03-20
Approval details
- PMA number
- P020025
- Supplement
- S144
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- IntellaNav MiFi XP Ablation Catheter
- Generic name
- catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
- Applicant
- Boston Scientific
- Date received
- 2025-03-07
- Decision date
- 2025-03-20
- Days to decision
- 13 days
- Decision code
- OK30
- Product code
- OAD
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- the transfer of manufacturing and packaging assembly operations for the IntellaNav MiFi XP and IntellaNav ST ablation catheters to the Coyol, Costa Rica facility
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