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MINI TIGHTROPE

Page Type
Cleared 510(K)
510(k) Number
K090107
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2009
Days to Decision
203 days
Submission Type
Summary

MINI TIGHTROPE

Page Type
Cleared 510(K)
510(k) Number
K090107
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2009
Days to Decision
203 days
Submission Type
Summary