PMA P060033S042
- Device
- ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
- Applicant
- Medtronic, Inc.
- PMA number
- P060033
- Supplement
- S042
- Product code
- NIQ
- Decision date
- 2009-10-30
- Generic name
- Coronary drug-eluting stent
- Approval order statement
- APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.
Current openFDA PMA Record
- Device
- ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
- Applicant
- Medtronic, Inc.
- PMA number
- P060033
- Supplement
- S042
- Product code
- NIQ
- Generic name
- Coronary drug-eluting stent
- Decision date
- 2009-10-30
- Decision code
- APPR
- Date received
- 2009-09-02
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Postapproval Study Protocol - OSB
- Approval order statement
- APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.