PMA P980033S018
- Device
- WALLSTENT (TIPS/LLIAC/VENOUS) ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S018
- Product code
- QKJ
- Decision date
- 2011-07-19
- Classification
- Stent, Coronary
- Generic name
- Stent, central venous
- Approval order statement
- APPROVAL FOR A COMPONENT VENDOR FACILITY SITE CHANGE.
Current openFDA PMA Record#
- Device
- WALLSTENT (TIPS/LLIAC/VENOUS) ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S018
- Product code
- QKJ
- Generic name
- Stent, central venous
- Decision date
- 2011-07-19
- Decision code
- APPR
- Date received
- 2011-02-10
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A COMPONENT VENDOR FACILITY SITE CHANGE.