PMA P960009S536

Device
Activa™ Deep Brain Stimulation Therapy System; Percept™ PC BrainSense™ (B35200)
Applicant
Medtronic, Inc.
PMA number
P960009
Supplement
S536
Product code
MHY
Decision date
2026-06-05
Classification
Neurology
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Approval order statement
for expansion of incoming electrolyte salt acceptance limits. Specifically, to expand LiAsF6 electrolyte salt moisture content acceptance limit from: = 100 parts per million (ppm) to: = 200 ppm and expand LiAsF6 electrolyte salt insoluble acceptance limit from: = 20 ppm to: = 200 ppm

Current openFDA PMA Record#

Device
Activa™ Deep Brain Stimulation Therapy System; Percept™ PC BrainSense™ (B35200)
Applicant
Medtronic, Inc.
PMA number
P960009
Supplement
S536
Product code
MHY
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Decision date
2026-06-05
Decision code
OK30
Date received
2026-05-08
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
for expansion of incoming electrolyte salt acceptance limits. Specifically, to expand LiAsF6 electrolyte salt moisture content acceptance limit from: = 100 parts per million (ppm) to: = 200 ppm and expand LiAsF6 electrolyte salt insoluble acceptance limit from: = 20 ppm to: = 200 ppm