FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Stent, Renal
PMA: P890017
·
Supplement: S022
·
Decision Mar 8, 2022
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Stent, Renal
- Trade Name
- Cordis® PALMAZ® Balloon-Expandable Stent
- PMA Number
- P890017
- Supplement Number
- S022
- 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
- March 8, 2022
- Date Received
- December 8, 2021
- Supplement Type
- Real-Time Process
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for updates to the MRI section in the Palmaz labeling and other minor labeling updates.
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 |