FDA PMA
Approved
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200015
·
Supplement: S063
·
Decision Jun 4, 2025
Classifications
1
FEI Numbers
14
Registration Numbers
14
Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Edwards SAPIEN 3 Pulmonic Delivery System: 9630PL29
- PMA Number
- P200015
- Supplement Number
- S063
- Product Code
- NPV
- Generic Name
- Pulmonary valve prosthesis percutaneously delivered
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 4, 2025
- Date Received
- March 28, 2025
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
approval for a manufacturing site located at Centerpiece S. de. R.L. de C.V., Bulevar La Encantada Industrial, Parque Industrial El Florido, Seccion La Encantada 11530, Tijuana, Baja California, 22250, Mexico for sterilization
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 |
|---|---|---|---|
| NPV | Pulmonary Valve Prosthesis Percutaneously Delivered | Unknown |