FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Stent, Central Venous
PMA: P980033
·
Supplement: S055
·
Decision Jul 25, 2019
Classifications
1
FEI Numbers
5
Registration Numbers
5
Basic Information
- Device Name
- Stent, Central Venous
- Trade Name
- WALLSTENT ENDOPROSTHESIS
- PMA Number
- P980033
- Supplement Number
- S055
- Device Class
- FDA Class 3
- Product Code
- QKJ
- Generic Name
- Stent, central venous
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 25, 2019
- Date Received
- June 27, 2019
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Replacement of the current software with new software to collect and process manufacturing test data, and track and trend capability data for various manufacturing areas.
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 |
|---|---|---|---|
| QKJ | Stent, Central Venous | FDA class 3 | Unknown |