PMA P980033S030
- Device
- WALLSTENT (VENOUS) ENDOPROSTHESIS
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S030
- Product code
- QKJ
- Decision date
- 2013-02-14
- Generic name
- Stent, central venous
- Approval order statement
- ADDITION OF A REWORK STEP IN THE ELECTRO ETCH PROCESS.
Current openFDA PMA Record#
- Device
- WALLSTENT (VENOUS) ENDOPROSTHESIS
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S030
- Product code
- QKJ
- Generic name
- Stent, central venous
- Decision date
- 2013-02-14
- Decision code
- OK30
- Date received
- 2013-01-15
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ADDITION OF A REWORK STEP IN THE ELECTRO ETCH PROCESS.