FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Appendage Closure, Left Atrial
PMA: P130013
·
Supplement: S056
·
Decision Jan 20, 2023
Classifications
1
FEI Numbers
13
Registration Numbers
13
Basic Information
- Device Name
- System, Appendage Closure, Left Atrial
- Trade Name
- WATCHMAN FLX Left Atrial Appendage Closure Device with Delivery System
- PMA Number
- P130013
- Supplement Number
- S056
- 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
- January 20, 2023
- Date Received
- October 25, 2022
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for an increase in the filter fabric length for each device size along with several other associated minor changes related to the increase in fabric length.
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 |