FDA 510(k) Applications Submitted by AMEDICA CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K082037	07/17/2008	SEEPLATE CERVICAL PLATE SYSTEM	AMEDICA CORP.
K073125	11/06/2007	VALEO VBR	AMEDICA CORP.
K073505	12/13/2007	MODIFICATION TO VALEO VBR	AMEDICA CORP.
K022729	08/16/2002	VENTED CEMENT RESTRICTOR	AMEDICA CORP.
K071990	07/20/2007	VALEO CERVICAL PLATE SYSTEM	AMEDICA CORP.
K173453	11/06/2017	Valeo« C+CSC with Lumen Interbody Fusion Device	Amedica Corp.
K072022	07/23/2007	VALEO PEDICLE SCREW SPINAL SYSTEM	AMEDICA CORP.
K073430	12/06/2007	VALEO PEDICLE SCREW SPINAL SYSTEM	AMEDICA CORP.
K050699	03/18/2005	MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004	AMEDICA CORP.
K091278	05/01/2009	VALEO SPACER SYSTEM	AMEDICA CORP.
K051525	06/08/2005	ARX SPINAL SYSTEM	AMEDICA CORP.
K121892	06/29/2012	PHANTOM PLUS CERAMIC CAGE SYSTEM	AMEDICA CORP.
K142264	08/15/2014	Valeo C Spacer System, Valeo II C IBF Device	Amedica Corp.
K161405	05/20/2016	Valeo II Interbody Fusion Device System	AMEDICA CORP.
K143518	12/12/2014	Valeo Spacer System and Valeo II Interbody Fusion Device System	Amedica Corp.