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Valeo® C+CSC with Lumen Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K173453
510(k) Type
Traditional
Applicant
Amedica Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2018
Days to Decision
119 days
Submission Type
Summary

Valeo® C+CSC with Lumen Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K173453
510(k) Type
Traditional
Applicant
Amedica Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2018
Days to Decision
119 days
Submission Type
Summary