PMA P980023S106

Device
Ilivia Neo 7 VR-T DX, Ilivia Neo 7 VR-T, Intica Neo 7 VR-T DX, Intica Neo 7 VR-T, Intica Neo 5 VR-T DX, Intica Neo 5 VR-
Applicant
Biotronik, Inc.
PMA number
P980023
Supplement
S106
Product code
LWS
Decision date
2021-07-21
Generic name
Implantable cardioverter defibrillator (non-CRT)
Approval order statement
Reduce incoming inspections on specified batteries, wiring bands, and resistors.

Current openFDA PMA Record#

Device
Ilivia Neo 7 VR-T DX, Ilivia Neo 7 VR-T, Intica Neo 7 VR-T DX, Intica Neo 7 VR-T, Intica Neo 5 VR-T DX, Intica Neo 5 VR-
Applicant
Biotronik, Inc.
PMA number
P980023
Supplement
S106
Product code
LWS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Decision date
2021-07-21
Decision code
OK30
Date received
2021-06-21
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Reduce incoming inspections on specified batteries, wiring bands, and resistors.