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ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM

Page Type
Cleared 510(K)
510(k) Number
K010525
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2001
Days to Decision
90 days
Submission Type
Summary

ARTHREX TENODESIS SCREW 7MM, 8MM, 9MM

Page Type
Cleared 510(K)
510(k) Number
K010525
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2001
Days to Decision
90 days
Submission Type
Summary