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MINI TIGHTROPE FT REPAIR KIT

Page Type
Cleared 510(K)
510(k) Number
K071978
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
28 days
Submission Type
Summary

MINI TIGHTROPE FT REPAIR KIT

Page Type
Cleared 510(K)
510(k) Number
K071978
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
28 days
Submission Type
Summary