FDA 510(k), K223269, Spencer Probe Depth Electrodes

FDA 510(k), K223269, Spencer Probe Depth Electrodes

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510(K) Number: K223269
Device Name: Spencer Probe Depth Electrodes
Manufacturer: Brendan McCrea
Device Classification Name: Electrode, Depth
Regulation Number: GZL
Classification Product Code: KXA
Date Received: 10/24/2022
Decision Date: 05/18/2023
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology

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