FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Appendage Closure, Left Atrial
PMA: P130013
·
Supplement: S060
·
Decision Dec 23, 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 (LAA) Closure Technology, WATCHMAN FLX Left Atrial Appendage Closure Device with Deli
- PMA Number
- P130013
- Supplement Number
- S060
- 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 23, 2023
- Date Received
- September 28, 2023
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for three laser cut toolpath updates impacting the design and manufacturing of implant frames for several sizes of the WATCHMAN FLX and WATCHMAN FLX Pro Left Atrial Appendage Closure Devices
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 |