FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Appendage Closure, Left Atrial
PMA: P130013
·
Supplement: S078
·
Decision Dec 15, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- System, Appendage Closure, Left Atrial
- Trade Name
- WATCHMAN FLX Pro Left Atrial Appendage Closure Device with Delivery System
- PMA Number
- P130013
- Supplement Number
- S078
- Device Class
- FDA Class 3
- Product Code
- NGV
- Generic Name
- System, appendage closure, left atrial
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 15, 2025
- Date Received
- August 14, 2025
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
the protocol for the post-approval study (PAS) referenced above
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 |
|---|---|---|---|
| NGV | System, Appendage Closure, Left Atrial | FDA class 3 | Unknown |