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Arthrex Knotless Mini TightRopes

Page Type
Cleared 510(K)
510(k) Number
K213644
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
29 days
Submission Type
Summary

Arthrex Knotless Mini TightRopes

Page Type
Cleared 510(K)
510(k) Number
K213644
510(k) Type
Special
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
29 days
Submission Type
Summary