FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stent, Renal
PMA: P890017
·
Supplement: S009
·
Decision Jul 11, 2000
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Stent, Renal
- Trade Name
- PALMAZ BALLOON EXPANDABLE STENT
- PMA Number
- P890017
- Supplement Number
- S009
- Device Class
- FDA Class 3
- Product Code
- NIN
- Generic Name
- STENT, RENAL
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- July 11, 2000
- Date Received
- May 26, 2000
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A REVISED INSTRUCTIONS FOR USE (IFU) FOR THE CORDIS PALMAZ(TM) BALLOON EXPANDABLE STENT.
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 |
|---|---|---|---|
| NIN | Stent, Renal | FDA class 3 | Unknown |