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LOW PROFILE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K103705
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2011
Days to Decision
88 days
Submission Type
Summary

LOW PROFILE SCREWS

Page Type
Cleared 510(K)
510(k) Number
K103705
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2011
Days to Decision
88 days
Submission Type
Summary