FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stent, Coronary
PMA: P020047
·
Supplement: S046
·
Decision Aug 20, 2012
Classifications
1
FEI Numbers
28
Registration Numbers
28
Basic Information
- Device Name
- Stent, Coronary
- Trade Name
- MULTI-LINK 8 AND MULTI-LINK 8 LL CORONARY STENT SYSTEM (CSS)
- PMA Number
- P020047
- Supplement Number
- S046
- 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
- August 20, 2012
- Date Received
- February 22, 2012
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A STERILIZATION SITE LOCATED IN TIPPERARY. IRELAND.
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 |