PMA P980016S779

Device
Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR/VR ICD, Evera XT DR/VR I
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P980016
Supplement
S779
Product code
LWS
Decision date
2021-04-12
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Process changes for the use of the dadet used in feedthrough assembly.

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/VR ICD, Evera XT DR/VR I
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P980016
Supplement
S779
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2021-04-12
Decision code
OK30
Date received
2021-03-16
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Process changes for the use of the dadet used in feedthrough assembly.