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ARIX Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K233912
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/11/2024
Days to Decision
90 days
Submission Type
Summary

ARIX Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K233912
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/11/2024
Days to Decision
90 days
Submission Type
Summary