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

FDA premarket approval P960009/S479 · decided 2024-05-23

Approval details

PMA number
P960009
Supplement
S479
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2024-05-17
Decision date
2024-05-23
Days to decision
6 days
Decision code
OK30
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
approval for the updates to the Delta 26H battery header tooling and associated processes in routine battery manufacturing at Medtronic’s internal supplier of batteries, Medtronic Energy and Component Center (MECC), Brooklyn Center, Minnesota

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