Atlas FDA

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

FDA premarket approval P960009/S455 · decided 2023-10-10

Approval details

PMA number
P960009
Supplement
S455
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2023-07-12
Decision date
2023-10-10
Days to decision
90 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
minor design and manufacturing changes to metal strip resistors, Specifically, 1) Change in construction from a copper clad technology to a welded copper technology; and 2) Change in resistor height requirement

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