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ARIX Ankle Distal Tibia System

Page Type
Cleared 510(K)
510(k) Number
K231887
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/14/2023
Days to Decision
170 days
Submission Type
Summary

ARIX Ankle Distal Tibia System

Page Type
Cleared 510(K)
510(k) Number
K231887
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/14/2023
Days to Decision
170 days
Submission Type
Summary