PMA P980033S029
- Device
- WALLSTENT RP ENDOPROSTHESIS AND WALLSTENT ENDOPROSTHESIS (VENOUS)
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S029
- Product code
- QKJ
- Decision date
- 2013-06-18
- Classification
- Stent, Coronary
- Generic name
- Stent, central venous
- Approval order statement
- APPROVAL FOR USE OF AN ALTERNATE PTFE MATERIAL.
Current openFDA PMA Record#
- Device
- WALLSTENT RP ENDOPROSTHESIS AND WALLSTENT ENDOPROSTHESIS (VENOUS)
- Applicant
- Boston Scientific Corporation
- PMA number
- P980033
- Supplement
- S029
- Product code
- QKJ
- Generic name
- Stent, central venous
- Decision date
- 2013-06-18
- Decision code
- APPR
- Date received
- 2012-11-27
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR USE OF AN ALTERNATE PTFE MATERIAL.