IntellaNav XP and IntellaNav MiFi XP Ablation Catheters
FDA premarket approval P020025/S143 · decided 2024-02-16
Approval details
- PMA number
- P020025
- Supplement
- S143
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- IntellaNav XP and IntellaNav MiFi XP Ablation Catheters
- Generic name
- catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
- Applicant
- Boston Scientific
- Date received
- 2023-11-21
- Decision date
- 2024-02-16
- Days to decision
- 87 days
- Decision code
- APPR
- Product code
- OAD
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Approval for changes to components in the Maestro Connection Box in order to meet the specifications
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