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Valeo II Interbody Fusion Device System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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