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

FDA premarket approval P960009/S449 · decided 2023-03-10

Approval details

PMA number
P960009
Supplement
S449
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, thalamic, epilepsy, implanted
Applicant
Medtronic, Inc.
Date received
2023-03-08
Decision date
2023-03-10
Days to decision
2 days
Decision code
OK30
Product code
MBX
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Update process monitoring controls (sample sizes and control limits) as part of the implementation of Statistical Process Control (SPC) program at Medtronic Vascular.

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