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Velofix Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190067
510(k) Type
Special
Applicant
U&i Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/4/2019
Days to Decision
20 days
Submission Type
Summary

Velofix Interbody Fusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190067
510(k) Type
Special
Applicant
U&i Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/4/2019
Days to Decision
20 days
Submission Type
Summary