PMA P010031S725

Device
Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D, Cobalt
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S725
Product code
NIK
Decision date
2020-12-16
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
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
Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D, Cobalt
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S725
Product code
NIK
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
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.