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VELOXTM INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140864
510(k) Type
Traditional
Applicant
U&I CORP.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/22/2014
Days to Decision
110 days
Submission Type
Summary

VELOXTM INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140864
510(k) Type
Traditional
Applicant
U&I CORP.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/22/2014
Days to Decision
110 days
Submission Type
Summary