FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Cardiac Ablation Percutaneous Catheter
PMA: P920047
·
Supplement: S124
·
Decision Aug 5, 2021
Classifications
1
FEI Numbers
52
Registration Numbers
52
Basic Information
- Device Name
- Cardiac Ablation Percutaneous Catheter
- Trade Name
- IntellaNav ST Ablation Catheter, Blazer II Temperature Ablation Catheter, Blazer II HTD Temperature Ablation Catheter, a
- PMA Number
- P920047
- Supplement Number
- S124
- Device Class
- FDA Class 3
- Product Code
- LPB
- Generic Name
- Cardiac ablation percutaneous catheter
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- August 5, 2021
- Date Received
- December 18, 2020
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for an adhesive change, minor manufacturing changes, and modification of a product specification.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LPB | Cardiac Ablation Percutaneous Catheter | FDA class 3 | Unknown |