FDA PMA
30-Day Notice Accepted
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200046
·
Supplement: S016
·
Decision May 23, 2023
Classifications
1
FEI Numbers
14
Registration Numbers
14
Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Harmony Transcatheter Pulmonic Valve System
- PMA Number
- P200046
- Supplement Number
- S016
- 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
- May 23, 2023
- Date Received
- May 9, 2023
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Addition of eddy current testing to check for nitinol wire surface defects at a nitinol wire sub-tier supplier.
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 |