FDA PMA
Approved
🇺🇸 United States
Pulmonary Valve Prosthesis Percutaneously Delivered
PMA: P200046
·
Supplement: S048
·
Decision Mar 6, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Pulmonary Valve Prosthesis Percutaneously Delivered
- Trade Name
- Harmony TPV System
- PMA Number
- P200046
- Supplement Number
- S048
- Product Code
- NPV
- Generic Name
- Pulmonary valve prosthesis percutaneously delivered
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 6, 2026
- Date Received
- February 4, 2026
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the revised protocols for PAS1, "Continued Follow-up of the Harmony TPV IDE Cohort," and PAS2, "Harmony TPV New Enrollment Study." The PAS protocols have been submitted to comply with the conditions of approval outlined in the approval order for P200046.
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 |