PMA P980016S742

Device
Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Intrinsic 30 ICD, M
Applicant
Medtronic Cardiac Rhythm Disease Management
Product code
LWS
Decision date
2020-07-24
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Approval for firmware updates to the MyCareLink Patient Monitor Model 24950

Current openFDA PMA Record#

Device
Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT DR ICD, Evera XT VR ICD, Intrinsic 30 ICD, M
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P980016
Supplement
S742
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2020-07-24
Decision code
APPR
Date received
2020-05-29
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Approval order statement
Approval for firmware updates to the MyCareLink Patient Monitor Model 24950