FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Iliac Covered Stent, Arterial
PMA: P160021
·
Supplement: S046
·
Decision Jun 18, 2024
Classifications
1
FEI Numbers
12
Registration Numbers
12
Basic Information
- Device Name
- Iliac Covered Stent, Arterial
- Trade Name
- GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis
- PMA Number
- P160021
- Supplement Number
- S046
- Device Class
- FDA Class 3
- Product Code
- PRL
- Generic Name
- Iliac covered stent, arterial
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 18, 2024
- Date Received
- June 17, 2024
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for removal of the compliance chart from the sterile pouch
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 |
|---|---|---|---|
| PRL | Iliac Covered Stent, Arterial | FDA class 3 | Unknown |