FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intracranial Aneurysm Flow Diverter
PMA: P170024
·
Supplement: S004
·
Decision Sep 14, 2020
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Intracranial Aneurysm Flow Diverter
- Trade Name
- Surpass Streamline Flow Diverter
- PMA Number
- P170024
- Supplement Number
- S004
- Device Class
- FDA Class 3
- Product Code
- OUT
- Generic Name
- Intracranial aneurysm flow diverter
- Medical Specialty
- Unknown
- Advisory Committee
- Neurology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 14, 2020
- Date Received
- June 2, 2020
- Supplement Type
- Real-Time Process
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for a shelf-life extension of the Surpass Streamline Flow Diverter from one year to three years.
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 |
|---|---|---|---|
| OUT | Intracranial Aneurysm Flow Diverter | FDA class 3 | Unknown |