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Amedica Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K173453Valeo® C+CSC with Lumen Interbody Fusion DeviceMarch 5, 2018
K161405Valeo II Interbody Fusion Device SystemAugust 19, 2016
K143518Valeo Spacer System and Valeo II Interbody Fusion Device SystemOctober 2, 2015
K142264Valeo C Spacer System, Valeo II C IBF DeviceDecember 8, 2014
K142347Amedica Valeo II Interbody Fusion DeviceNovember 18, 2014
K121892PHANTOM PLUS CERAMIC CAGE SYSTEMAugust 24, 2012
K091278VALEO SPACER SYSTEMJanuary 28, 2010
K082037SEEPLATE CERVICAL PLATE SYSTEMSeptember 26, 2008
K073430VALEO PEDICLE SCREW SPINAL SYSTEMJanuary 29, 2008
K073505MODIFICATION TO VALEO VBRJanuary 9, 2008
K073125VALEO VBRDecember 5, 2007
K072022VALEO PEDICLE SCREW SPINAL SYSTEMNovember 19, 2007
K071990VALEO CERVICAL PLATE SYSTEMOctober 29, 2007
K051525ARX SPINAL SYSTEMFebruary 17, 2006
K050699MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004April 15, 2005
K022729VENTED CEMENT RESTRICTORNovember 14, 2002