FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Appendage Closure, Left Atrial
PMA: P130013
·
Supplement: S054
·
Decision Oct 28, 2022
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
- S054
- 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
- October 28, 2022
- Date Received
- September 29, 2022
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the protocol for the post-approval study (PAS) protocol.
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 |