FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Transcatheter Septal Occluder
PMA: P120021
·
Supplement: S023
·
Decision Dec 22, 2021
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Transcatheter Septal Occluder
- Trade Name
- AmplatzerTM PFO Occluder and AmplatzerTM TalismanTM PFO Occluder
- PMA Number
- P120021
- Supplement Number
- S023
- Device Class
- FDA Class 3
- Product Code
- MLV
- Generic Name
- Transcatheter septal occluder
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 22, 2021
- Date Received
- November 26, 2021
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the revised 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 |
|---|---|---|---|
| MLV | Transcatheter Septal Occluder | FDA class 3 | Unknown |