FDA PMA
30-Day Notice Accepted
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200015
·
Supplement: S075
·
Decision Mar 11, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Edwards SAPIEN 3 Transcatheter Heart Valve
- PMA Number
- P200015
- Supplement Number
- S075
- Product Code
- NPV
- Generic Name
- Pulmonary valve prosthesis percutaneously delivered
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- March 11, 2026
- Date Received
- February 10, 2026
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
alternate suppliers of solutions used in the manufacturing process of transcatheter and surgical heart valves
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 |