PMA P060033S048

Device
ENDEAVOR SPRINT ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
Applicant
Medtronic, Inc.
PMA number
P060033
Supplement
S048
Product code
NIQ
Decision date
2010-02-26
Generic name
Coronary drug-eluting stent
Approval order statement
CHANGE TO THE INITIAL CRIMP STENT PROCESS.

Current openFDA PMA Record

Device
ENDEAVOR SPRINT ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM
Applicant
Medtronic, Inc.
PMA number
P060033
Supplement
S048
Product code
NIQ
Generic name
Coronary drug-eluting stent
Decision date
2010-02-26
Decision code
OK30
Date received
2009-01-25
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
CHANGE TO THE INITIAL CRIMP STENT PROCESS.

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