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Arthrex TightRope II

Page Type
Cleared 510(K)
510(k) Number
K231857
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2023
Days to Decision
46 days
Submission Type
Summary

Arthrex TightRope II

Page Type
Cleared 510(K)
510(k) Number
K231857
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2023
Days to Decision
46 days
Submission Type
Summary