Medical Device Manufacturer · US , Salt Lake City , UT

Amedica Corp. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 2002
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.

FDA 510(k) Regulatory Record - Amedica Corp.
16 devices
1-12 of 16
Cleared Mar 05, 2018
Valeo® C+CSC with Lumen Interbody Fusion Device
K173453 · ODP
Orthopedic · 119d
Cleared Aug 19, 2016
Valeo II Interbody Fusion Device System
K161405 · MAX
Orthopedic · 91d
Cleared Oct 02, 2015
Valeo Spacer System and Valeo II Interbody Fusion Device System
K143518 · MAX
Orthopedic · 294d
Cleared Dec 08, 2014
Valeo C Spacer System, Valeo II C IBF Device
K142264 · ODP
Orthopedic · 115d
Cleared Nov 18, 2014
Amedica Valeo II Interbody Fusion Device
K142347 · MAX
Orthopedic · 88d
Cleared Aug 24, 2012
PHANTOM PLUS CERAMIC CAGE SYSTEM
K121892 · MAX
Orthopedic · 56d
Cleared Jan 28, 2010
VALEO SPACER SYSTEM
K091278 · MAX
Orthopedic · 272d
Cleared Sep 26, 2008
SEEPLATE CERVICAL PLATE SYSTEM
K082037 · KWQ
Orthopedic · 71d
Cleared Jan 29, 2008
VALEO PEDICLE SCREW SPINAL SYSTEM
K073430 · NKB
Orthopedic · 54d
Cleared Jan 09, 2008
MODIFICATION TO VALEO VBR
K073505 · MQP
Orthopedic · 27d
Cleared Dec 05, 2007
VALEO VBR
K073125 · MQP
Orthopedic · 29d
Cleared Nov 19, 2007
VALEO PEDICLE SCREW SPINAL SYSTEM
K072022 · NKB
Orthopedic · 119d
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