PMA P110019S012
- Device
- XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM & XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM
- Applicant
- Abbott Vascular
- PMA number
- P110019
- Supplement
- S012
- Product code
- NIQ
- Decision date
- 2012-03-02
- Classification
- Coronary Drug-eluting Stent
- Generic name
- Coronary drug-eluting stent
- Approval order statement
- EQUIPMENT UPGRADE FOR USE IN THE STENT RETENTION PROCESS.
Current openFDA PMA Record#
- Device
- XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM & XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM
- Applicant
- Abbott Vascular
- PMA number
- P110019
- Supplement
- S012
- Product code
- NIQ
- Generic name
- Coronary drug-eluting stent
- Decision date
- 2012-03-02
- Decision code
- OK30
- Date received
- 2012-02-03
- Supplement type
- 30-Day Notice
- Approval order statement
- EQUIPMENT UPGRADE FOR USE IN THE STENT RETENTION PROCESS.