FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stent, Carotid
PMA: P040012
·
Supplement: S018
·
Decision Oct 2, 2006
Classifications
1
FEI Numbers
24
Registration Numbers
24
Basic Information
- Device Name
- Stent, Carotid
- Trade Name
- RX ACCULINK AND ACCULINK CAROTID STENT SYSTEMS
- PMA Number
- P040012
- Supplement Number
- S018
- Device Class
- FDA Class 3
- Product Code
- NIM
- Generic Name
- Stent, carotid
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- October 2, 2006
- Date Received
- July 10, 2006
- Supplement Type
- 135 Review Track For 30-Day Notice
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A CHANGE IN THE METHOD OF INSPECTING THE ACCULINK STENT OUTER DIAMETER.
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 |
|---|---|---|---|
| NIM | Stent, Carotid | FDA class 3 | Unknown |