FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Stent, Renal
PMA: P890017
·
Supplement: S015
·
Decision Oct 30, 2009
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
- S015
- Device Class
- FDA Class 3
- Product Code
- NIN
- Generic Name
- STENT, RENAL
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 30, 2009
- Date Received
- October 1, 2009
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
DISCONTINUANCE OF A REDUNDANT INSPECTION.
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 |