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Arthrex FiberTape Cerclage

Page Type
Cleared 510(K)
510(k) Number
K170206
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2017
Days to Decision
295 days
Submission Type
Summary

Arthrex FiberTape Cerclage

Page Type
Cleared 510(K)
510(k) Number
K170206
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2017
Days to Decision
295 days
Submission Type
Summary