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SYNTHES VA LCP ANKLE TRAUMA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120854
510(k) Type
Traditional
Applicant
SYNTHES USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2012
Days to Decision
89 days
Submission Type
Summary

SYNTHES VA LCP ANKLE TRAUMA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120854
510(k) Type
Traditional
Applicant
SYNTHES USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2012
Days to Decision
89 days
Submission Type
Summary