PMA P050023S215

Device
Ilivia 7 VR-T DX DF-1 ProMRI Ilivia 7 VR-T DF-1 ProMRI Ilivia 7 VR-T DF4 ProMRI Intica 7 VR-T DX DF-1 ProMRI Intica 7 VR
Applicant
Biotronik, Inc.
PMA number
P050023
Supplement
S215
Product code
MRM
Decision date
2026-10-13
Classification
Cardiovascular
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Approval order statement
a change to the rework process for the manufacturing of the housing for pulse generators and ICDS

Current openFDA PMA Record#

Device
Ilivia 7 VR-T DX DF-1 ProMRI Ilivia 7 VR-T DF-1 ProMRI Ilivia 7 VR-T DF4 ProMRI Intica 7 VR-T DX DF-1 ProMRI Intica 7 VR
Applicant
Biotronik, Inc.
PMA number
P050023
Supplement
S215
Product code
MRM
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Decision date
2026-10-13
Decision code
OK30
Date received
2026-09-18
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
a change to the rework process for the manufacturing of the housing for pulse generators and ICDS