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Arthrex Patella SuturePlates

Page Type
Cleared 510(K)
510(k) Number
K203834
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2021
Days to Decision
85 days
Submission Type
Summary

Arthrex Patella SuturePlates

Page Type
Cleared 510(K)
510(k) Number
K203834
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2021
Days to Decision
85 days
Submission Type
Summary