Amedica Corp. is one of 13754 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amedica Corp. - FDA 510(k) Cleared Devices
Recent clearances: Valeo® C+CSC with Lumen Interbody Fusion Device, Valeo II Interbody Fusion Device System, Valeo Spacer System and Valeo II Interbody Fusion Device System
16
Total
16
Cleared
0
Denied
Amedica Corp. has 16 FDA 510(k) cleared orthopedic devices. Based in Salt Lake City, US.
Historical record: 16 cleared submissions from 2002 to 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and Shanna Ryan.
FDA 510(k) Regulatory Record - Amedica Corp.
16 devices
Cleared
Mar 05, 2018
Valeo® C+CSC with Lumen Interbody Fusion Device
Orthopedic
119d
Cleared
Aug 19, 2016
Valeo II Interbody Fusion Device System
Orthopedic
91d
Cleared
Oct 02, 2015
Valeo Spacer System and Valeo II Interbody Fusion Device System
Orthopedic
294d
Cleared
Dec 08, 2014
Valeo C Spacer System, Valeo II C IBF Device
Orthopedic
115d
Cleared
Nov 18, 2014
Amedica Valeo II Interbody Fusion Device
Orthopedic
88d
Cleared
Aug 24, 2012
PHANTOM PLUS CERAMIC CAGE SYSTEM
Orthopedic
56d
Cleared
Jan 28, 2010
VALEO SPACER SYSTEM
Orthopedic
272d
Cleared
Sep 26, 2008
SEEPLATE CERVICAL PLATE SYSTEM
Orthopedic
71d
Cleared
Jan 29, 2008
VALEO PEDICLE SCREW SPINAL SYSTEM
Orthopedic
54d
Cleared
Jan 09, 2008
MODIFICATION TO VALEO VBR
Orthopedic
27d
Cleared
Dec 05, 2007
VALEO VBR
Orthopedic
29d
Cleared
Nov 19, 2007
VALEO PEDICLE SCREW SPINAL SYSTEM
Orthopedic
119d