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Amedica Corp.

16 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Valeo® C+CSC with Lumen Interbody Fusion Device (K173453)Amedica Corp.2018-03-05
Valeo II Interbody Fusion Device System (K161405)Amedica Corp.2016-08-19
Valeo Spacer System and Valeo II Interbody Fusion Device System (K143518)Amedica Corp.2015-10-02
Valeo C Spacer System, Valeo II C IBF Device (K142264)Amedica Corp.2014-12-08
Amedica Valeo II Interbody Fusion Device (K142347)Amedica Corp.2014-11-18
PHANTOM PLUS CERAMIC CAGE SYSTEM (K121892)Amedica Corp.2012-08-24
VALEO SPACER SYSTEM (K091278)Amedica Corp.2010-01-28
SEEPLATE CERVICAL PLATE SYSTEM (K082037)Amedica Corp.2008-09-26
VALEO PEDICLE SCREW SPINAL SYSTEM (K073430)Amedica Corp.2008-01-29
MODIFICATION TO VALEO VBR (K073505)Amedica Corp.2008-01-09
VALEO VBR (K073125)Amedica Corp.2007-12-05
VALEO PEDICLE SCREW SPINAL SYSTEM (K072022)Amedica Corp.2007-11-19
VALEO CERVICAL PLATE SYSTEM (K071990)Amedica Corp.2007-10-29
ARX SPINAL SYSTEM (K051525)Amedica Corp.2006-02-17
MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004 (K050699)Amedica Corp.2005-04-15
VENTED CEMENT RESTRICTOR (K022729)Amedica Corp.2002-11-14

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