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ANTHREX TITANIUM OPENING WEDGE OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032187
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2003
Days to Decision
67 days
Submission Type
Summary

ANTHREX TITANIUM OPENING WEDGE OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032187
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2003
Days to Decision
67 days
Submission Type
Summary