Atlas FDA

Master Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™

FDA premarket approval P960009/S462 · decided 2023-12-12

Approval details

PMA number
P960009
Supplement
S462
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Master Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2023-09-13
Decision date
2023-12-12
Days to decision
90 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
to deploy a new Commercial Off-the-Shelf (COTS) tool, Samsung’s Enterprise Firmware Over the Air (EFOTA) to the Clinician Tablet so that the Android Operating System updates can be deployed as needed by Medtronic.

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