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Arthrex SutureTape

Page Type
Cleared 510(K)
510(k) Number
K221354
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2022
Days to Decision
122 days
Submission Type
Summary

Arthrex SutureTape

Page Type
Cleared 510(K)
510(k) Number
K221354
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2022
Days to Decision
122 days
Submission Type
Summary