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Arthrex Knee Systems

Page Type
Cleared 510(K)
510(k) Number
K171365
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
182 days
Submission Type
Summary

Arthrex Knee Systems

Page Type
Cleared 510(K)
510(k) Number
K171365
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2017
Days to Decision
182 days
Submission Type
Summary