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ARIX Humerus System

Page Type
Cleared 510(K)
510(k) Number
K172008
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/1/2017
Days to Decision
151 days
Submission Type
Summary

ARIX Humerus System

Page Type
Cleared 510(K)
510(k) Number
K172008
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/1/2017
Days to Decision
151 days
Submission Type
Summary