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FiberTak DR

Page Type
Cleared 510(K)
510(k) Number
K160319
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
95 days
Submission Type
Summary

FiberTak DR

Page Type
Cleared 510(K)
510(k) Number
K160319
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2016
Days to Decision
95 days
Submission Type
Summary