FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Stent, Carotid
PMA: P030047
·
Supplement: S015
·
Decision Oct 30, 2008
Classifications
1
FEI Numbers
24
Registration Numbers
24
Basic Information
- Device Name
- Stent, Carotid
- Trade Name
- PRECISE NITINOL STENT SYSTEM
- PMA Number
- P030047
- Supplement Number
- S015
- Device Class
- FDA Class 3
- Product Code
- NIM
- Generic Name
- Stent, carotid
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 30, 2008
- Date Received
- September 29, 2008
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
CHANGE TO THE TEST METHOD FOR A DELIVERY SYSTEM COMPONENT USED IN THE MANUFACTURE OF THE DEVICE.
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 |
|---|---|---|---|
| NIM | Stent, Carotid | FDA class 3 | Unknown |