PMA P010031S913

Device
Cobalt MRI CRT-D; Cobalt XT MRI CRT-D; Crome MRI CRT-D
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S913
Product code
NIK
Decision date
2026-01-16
Classification
Cardiovascular
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Approval order statement
to implement an additional manufacturing step for lithium strips used in battery anodes

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
S913
Product code
NIK
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Decision date
2026-01-16
Decision code
OK30
Date received
2026-01-07
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
to implement an additional manufacturing step for lithium strips used in battery anodes