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ARTHREX COMPRESSION FT SCREWS

Page Type
Cleared 510(K)
510(k) Number
K132217
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2013
Days to Decision
131 days
Submission Type
Summary

ARTHREX COMPRESSION FT SCREWS

Page Type
Cleared 510(K)
510(k) Number
K132217
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2013
Days to Decision
131 days
Submission Type
Summary