PMA P980016S763

Device
Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Eve
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P980016
Supplement
S763
Product code
LWS
Decision date
2020-12-16
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Implement a new software check system that occurs after the wafer test steps at Medtronic Tempe Campus.

Current openFDA PMA Record#

Device
Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Eve
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P980016
Supplement
S763
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2020-12-16
Decision code
OK30
Date received
2020-11-19
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Implement a new software check system that occurs after the wafer test steps at Medtronic Tempe Campus.