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Activa™ and Percept™ Deep Brain Stimulation Therapy System

FDA premarket approval P960009/S503 · decided 2025-06-10

Approval details

PMA number
P960009
Supplement
S503
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Activa™ and Percept™ Deep Brain Stimulation Therapy System
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2025-03-13
Decision date
2025-06-10
Days to decision
89 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
approval for a change to the sterile barrier packaging of the model 3550-68 twist-lock screening cable kit. The screening cable kit is currently packaged in a blister tray with sealed lid that is then placed into an outer pouch, and this change proposes removal of the outer pouch.

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