PMA P960009S530

Device
Activa™ Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™
Applicant
Medtronic, Inc.
PMA number
P960009
Supplement
S530
Product code
MHY
Decision date
2026-02-27
Classification
Neurology
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Approval order statement
to implement a new Keyence Inspection System for the battery electrode compression process set-up

Current openFDA PMA Record#

Device
Activa™ Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™
Applicant
Medtronic, Inc.
PMA number
P960009
Supplement
S530
Product code
MHY
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Decision date
2026-02-27
Decision code
OK30
Date received
2026-01-30
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
to implement a new Keyence Inspection System for the battery electrode compression process set-up