FDA 510(k) Application Details - K163317

Device Classification Name	Controller, Foot, Handpiece And Cord   More FDA Info for this Device
510(K) Number	K163317
Device Name	Controller, Foot, Handpiece And Cord
Applicant	Kaltenbach & Voigt GmgH Bismarckring 39 Biberach 88400 DE Other 510(k) Applications for this Company
Contact	Stefan Trampler Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/23/2016
Decision Date	02/21/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review