PMA P980033S039
- Device
- WALLSTENT (VENOUS)ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S039
- Product code
- QKJ
- Decision date
- 2013-12-20
- Generic name
- Stent, central venous
- Approval order statement
- ELIMINATE AN IN-PROCESS VERIFICATION ACTIVITY.
Current openFDA PMA Record#
- Device
- WALLSTENT (VENOUS)ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S039
- Product code
- QKJ
- Generic name
- Stent, central venous
- Decision date
- 2013-12-20
- Decision code
- OK30
- Date received
- 2013-11-25
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ELIMINATE AN IN-PROCESS VERIFICATION ACTIVITY.