FDA 510(k) Application Details - K163405

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K163405
Device Name	System, Image Processing, Radiological
Applicant	Kico Knee Innovation Company PTY Limited Suite 3, Building 1, 20 Bridge Street Pymble 2073 AU Other 510(k) Applications for this Company
Contact	Karl Rentsch Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2016
Decision Date	03/21/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review