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Valeo II Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K161405
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2016
Days to Decision
91 days
Submission Type
Summary

Valeo II Interbody Fusion Device System

Page Type
Cleared 510(K)
510(k) Number
K161405
510(k) Type
Special
Applicant
AMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2016
Days to Decision
91 days
Submission Type
Summary