PMA P980016S802

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
Product code
LWS
Decision date
2022-01-31
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Modifications to the plasma cleaning process at Medtronic's internal supplier.

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
S802
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2022-01-31
Decision code
OK30
Date received
2022-01-10
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Modifications to the plasma cleaning process at Medtronic's internal supplier.