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ARTHERX CORKSCREW FT II SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K050358
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2005
Days to Decision
60 days
Submission Type
Summary

ARTHERX CORKSCREW FT II SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K050358
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2005
Days to Decision
60 days
Submission Type
Summary