FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stent, Coronary
PMA: P970061
·
Supplement: S004
·
Decision Sep 25, 1998
Classifications
1
FEI Numbers
28
Registration Numbers
28
Basic Information
- Device Name
- Stent, Coronary
- Trade Name
- SCIMED RADIUS CORONARY STENT WITH DELIVERY SYSTEM
- PMA Number
- P970061
- Supplement Number
- S004
- Device Class
- FDA Class 3
- Product Code
- MAF
- Generic Name
- STENT, CORONARY
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 25, 1998
- Date Received
- September 4, 1998
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for revisions to the Instructions for Use.
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 |
|---|---|---|---|
| MAF | Stent, Coronary | FDA class 3 | Unknown |