FDA PMA
Approved
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200015
·
Supplement: S028
·
Decision Jan 19, 2023
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
- PMA Number
- P200015
- Supplement Number
- S028
- Product Code
- NPV
- Generic Name
- Pulmonary valve prosthesis percutaneously delivered
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 19, 2023
- Date Received
- August 31, 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 adding an alternate supplier for the balloon shaft component of the Edwards Pulmonic Delivery System.
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 |