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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.
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