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Veloxion System

Page Type
Cleared 510(K)
510(k) Number
K162979
510(k) Type
Traditional
Applicant
Corinth Medtech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
149 days
Submission Type
Summary

Veloxion System

Page Type
Cleared 510(K)
510(k) Number
K162979
510(k) Type
Traditional
Applicant
Corinth Medtech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2017
Days to Decision
149 days
Submission Type
Summary