FDA 510(k) Application Details - K173931

Device Classification Name	System, Optical Position/Movement Recording   More FDA Info for this Device
510(K) Number	K173931
Device Name	System, Optical Position/Movement Recording
Applicant	MindMaze SA Chemin de Roseneck 5 Lausanne CH-1006 CH Other 510(k) Applications for this Company
Contact	Sylvian Bourriquet Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/26/2017
Decision Date	05/17/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review