PMA P060033S080

Device
ENDEAVOR SPRINT ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
Applicant
Medtronic, Inc.
PMA number
P060033
Supplement
S080
Product code
NIQ
Decision date
2013-09-18
Generic name
Coronary drug-eluting stent
Approval order statement
CHANGE TO THE LABELING INSPECTION PROCESS.

Current openFDA PMA Record#

Device
ENDEAVOR SPRINT ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
Applicant
Medtronic, Inc.
PMA number
P060033
Supplement
S080
Product code
NIQ
Generic name
Coronary drug-eluting stent
Decision date
2013-09-18
Decision code
OK30
Date received
2013-08-19
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
CHANGE TO THE LABELING INSPECTION PROCESS.