FDA 510(k), K091457, NEXSTIM EXIMIA NAVIGATED BRAIN STIMULATION SYSTEM

FDA 510(k), K091457, NEXSTIM EXIMIA NAVIGATED BRAIN STIMULATION SYSTEM

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510(K) Number: K091457
Device Name: NEXSTIM EXIMIA NAVIGATED BRAIN STIMULATION SYSTEM
Manufacturer:
Device Classification Name: Stimulator, Electrical, Evoked Response
Regulation Number: 882.1870
Classification Product Code: GWF
Date Received: 05/18/2009
Decision Date: 12/08/2009
Regulation Medical Specialty: Neurology
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