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ACL TIGHTROPE,ACL TIGHTROPE DUUBLE BUNDLE

Page Type
Cleared 510(K)
510(k) Number
K112990
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2011
Days to Decision
74 days
Submission Type
Summary

ACL TIGHTROPE,ACL TIGHTROPE DUUBLE BUNDLE

Page Type
Cleared 510(K)
510(k) Number
K112990
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2011
Days to Decision
74 days
Submission Type
Summary