PMA P010031S879

Device
Cobalt MRI CRT-D, Cobalt XT MRI CRT-D, Crome MRI CRT-D
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S879
Product code
NIK
Decision date
2025-06-05
Classification
Cardiovascular
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Approval order statement
approval for an update to the transition tooling used in Cobalt/Crome device battery manufacturing

Current openFDA PMA Record#

Device
Cobalt MRI CRT-D, Cobalt XT MRI CRT-D, Crome MRI CRT-D
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S879
Product code
NIK
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Decision date
2025-06-05
Decision code
APPR
Date received
2024-12-20
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
approval for an update to the transition tooling used in Cobalt/Crome device battery manufacturing