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SYNTHES (USA) 3.5MM LCP POSTEROMEDIAL PROXIMAL TIBIA PLATES

Page Type
Cleared 510(K)
510(k) Number
K082624
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2008
Days to Decision
62 days
Submission Type
Summary

SYNTHES (USA) 3.5MM LCP POSTEROMEDIAL PROXIMAL TIBIA PLATES

Page Type
Cleared 510(K)
510(k) Number
K082624
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2008
Days to Decision
62 days
Submission Type
Summary