FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Cardiac Ablation Percutaneous Catheter
PMA: P990071
·
Supplement: S067
·
Decision Sep 15, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Cardiac Ablation Percutaneous Catheter
- Trade Name
- SMARTABLATE System Interface Cable (D-1303-02-S)
- PMA Number
- P990071
- Supplement Number
- S067
- Device Class
- FDA Class 3
- Product Code
- LPB
- Generic Name
- Cardiac ablation percutaneous catheter
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- September 15, 2025
- Date Received
- August 22, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
an alternative subassembly manufacturer for the SMARTABALTE System Interface Cable (D-1303-02-S)
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 |