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Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm Module

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191326
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
152 days
Submission Type
Summary

Arthrex Mini Comprehensive Fixation System – 1.4mm & 1.6mm Module

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191326
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2019
Days to Decision
152 days
Submission Type
Summary