# Amedica Corp.

- Location (FDA's records): Slat Lake City, UT
- FDA decisions: 17 (2002–2018): 17 510(k) clearances
- Names in FDA's records: Amedica Corp. (16); Amedica Corporation (1)
- Product codes: MAX (5), MQP (3), NKB (3), ODP (2), KWQ (2), JDK (1), JDX (1)
- 510(k) review time since 2016: median 108 days, against 124 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 53 (14 its own); citations of its devices by later devices: 37 (14 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Sofamor Danek: 5 (https://510kreport.com/company/medtronic-sofamor-danek)
- Ebi, L.P.: 3 (https://510kreport.com/company/ebi)
- U&I Corp., America: 3 (https://510kreport.com/company/u-i-america)
- Globus Medical, Inc.: 2 (https://510kreport.com/company/globus-medical)
- Us Spine: 2 (https://510kreport.com/company/us-spine)
- Jemo Spine, LLC: 2 (https://510kreport.com/company/jemo-spine)
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)

## Firms that cite its devices most
- Ctl Medical Corporation: 7 (https://510kreport.com/company/ctl-medical)
- Medacta International S.A.: 4 (https://510kreport.com/company/medacta-international)
- Orthomod, LLC: 1 (https://510kreport.com/company/orthomod)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Ackermann Instrumente GmbH: 1 (https://510kreport.com/company/ackermann-instrumente)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Paradigm Spine, LLC: 1 (https://510kreport.com/company/paradigm-spine)

## Its most-cited devices
- K142264: Valeo C Spacer System, Valeo II C IBF Device (2014), cited by 8
- K072022: Valeo Pedicle Screw Spinal System (2007), cited by 7
- K091278: Valeo Spacer System (2010), cited by 4
- K143518: Valeo Spacer System and Valeo II Interbody Fusion Device System (2015), cited by 3
- K121892: Phantom Plus Ceramic Cage System (2012), cited by 3
- K161405: Valeo II Interbody Fusion Device System (2016), cited by 2

## Recent decisions
- K173453: Valeo® C+CSC with Lumen Interbody Fusion Device (Mar 5, 2018)
- K162160: Preference Elite Pedicle Screw System (Nov 18, 2016)
- K161405: Valeo II Interbody Fusion Device System (Aug 19, 2016)
- K143518: Valeo Spacer System and Valeo II Interbody Fusion Device System (Oct 2, 2015)
- K142264: Valeo C Spacer System, Valeo II C IBF Device (Dec 8, 2014)
- K142347: Amedica Valeo II Interbody Fusion Device (Nov 18, 2014)
- K121892: Phantom Plus Ceramic Cage System (Aug 24, 2012)
- K091278: Valeo Spacer System (Jan 28, 2010)

Source page: https://510kreport.com/company/amedica