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ARIX Cannulated Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192417
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/26/2019
Days to Decision
83 days
Submission Type
Summary

ARIX Cannulated Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192417
510(k) Type
Traditional
Applicant
Jeil Medical Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/26/2019
Days to Decision
83 days
Submission Type
Summary