PMA P010031S930

Device
Amplia MRI CRT-D (DTMB1D1, DTMB1D4); Amplia MRI Quad CRT-D (DTMB1Q1, DTMB1QQ); Brava CRT-D (DTBC1D1, DTBC1D4) Brava Quad
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S930
Product code
NIK
Decision date
2026-07-31
Classification
Cardiovascular
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Approval order statement
to update test methodology and parameters for screening of integrated circuits used in Implantable Cardioverter-Defibrillators and Cardiac Resynchronization Therapy Defibrillators

Current openFDA PMA Record#

Device
Amplia MRI CRT-D (DTMB1D1, DTMB1D4); Amplia MRI Quad CRT-D (DTMB1Q1, DTMB1QQ); Brava CRT-D (DTBC1D1, DTBC1D4) Brava Quad
Applicant
Medtronic Cardiac Rhythm Disease Management
PMA number
P010031
Supplement
S930
Product code
NIK
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Decision date
2026-07-31
Decision code
OK30
Date received
2026-07-15
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
to update test methodology and parameters for screening of integrated circuits used in Implantable Cardioverter-Defibrillators and Cardiac Resynchronization Therapy Defibrillators