PMA P100023S083
- Device
- ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
- Applicant
- Boston Scientific Corp
- PMA number
- P100023
- Supplement
- S083
- Product code
- NIQ
- Decision date
- 2014-02-06
- Generic name
- Coronary drug-eluting stent
- Approval order statement
- CHANGE TO THE DELIVERY CATHETER ASSEMBLY MANUFACTURING PROCESS.
Current openFDA PMA Record
- Device
- ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
- Applicant
- Boston Scientific Corp
- PMA number
- P100023
- Supplement
- S083
- Product code
- NIQ
- Generic name
- Coronary drug-eluting stent
- Decision date
- 2014-02-06
- Decision code
- OK30
- Date received
- 2014-01-08
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE TO THE DELIVERY CATHETER ASSEMBLY MANUFACTURING PROCESS.