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

FDA premarket approval P960009/S419 · decided 2022-04-06

Approval details

PMA number
P960009
Supplement
S419
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
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
2022-01-26
Decision date
2022-04-06
Days to decision
70 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for an update to the primary Information for Prescribers (IFP) clinician labeling, and update to the primary Patient Therapy Guide (PTG) to mitigate the potential for implantable neurostimulator (INS) malfunction during a cardioversion procedure.

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