FDA PMA
30-Day Notice Accepted
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200046
·
Supplement: S036
·
Decision Feb 12, 2025
Classifications
1
FEI Numbers
14
Registration Numbers
14
Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Harmony Transcatheter Pulmonary Valve
- PMA Number
- P200046
- Supplement Number
- S036
- 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
- February 12, 2025
- Date Received
- January 21, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
layout changes, updated environmental monitoring plan, personnel capacity and the operational, action and alert limits for non-viable air particles andsurface monitoring for two controlled environment areas (CEA)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 |
|---|---|---|---|
| NPV | Pulmonary Valve Prosthesis Percutaneously Delivered | Unknown |