FDA PMA
Approved
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200015
·
Supplement: S018
·
Decision Nov 16, 2022
Classifications
1
FEI Numbers
14
Registration Numbers
14
Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Edwards SAPIEN 3 Transcatheter Heart Valve
- PMA Number
- P200015
- Supplement Number
- S018
- Product Code
- NPV
- Generic Name
- Pulmonary valve prosthesis percutaneously delivered
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- November 16, 2022
- Date Received
- March 18, 2022
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Approval for an alternate supplier of a component of the solution used for in-process bioburden reduction.
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 |