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SYNTHES LCP ANKLE ARTHRODESIS PLATES

Page Type
Cleared 510(K)
510(k) Number
K061940
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2006
Days to Decision
60 days
Submission Type
Summary

SYNTHES LCP ANKLE ARTHRODESIS PLATES

Page Type
Cleared 510(K)
510(k) Number
K061940
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2006
Days to Decision
60 days
Submission Type
Summary