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Velofix(tm) Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171749
510(k) Type
Traditional
Applicant
U&i Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/13/2017
Days to Decision
30 days
Submission Type
Summary

Velofix(tm) Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171749
510(k) Type
Traditional
Applicant
U&i Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/13/2017
Days to Decision
30 days
Submission Type
Summary