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ARTHREX CANNULATED INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K915424
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1993
Days to Decision
435 days
Submission Type
Statement

ARTHREX CANNULATED INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K915424
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1993
Days to Decision
435 days
Submission Type
Statement