FDA 510(k) Application Details - K172444

Device Classification Name	Neurological Stereotaxic Instrument   More FDA Info for this Device
510(K) Number	K172444
Device Name	Neurological Stereotaxic Instrument
Applicant	MEDTECH S.A. ZAC Eureka - 900 Rue Du Mas De Verchant Montpellier 34000 FR Other 510(k) Applications for this Company
Contact	Elise Lagacherie Other 510(k) Applications for this Contact
Regulation Number	882.4560   More FDA Info for this Regulation Number
Classification Product Code	HAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/14/2017
Decision Date	03/28/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review