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SYNTHES 3.5 MM LCP DISTAL TIBIA T PLATES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080522
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
87 days
Submission Type
Summary

SYNTHES 3.5 MM LCP DISTAL TIBIA T PLATES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080522
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2008
Days to Decision
87 days
Submission Type
Summary