Last synced on 18 April 2025 at 11:05 pm

SYNTHES 2.7 MM/3.5 MM LCP DISTAL FIBULA PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083213
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2008
Days to Decision
60 days
Submission Type
Summary

SYNTHES 2.7 MM/3.5 MM LCP DISTAL FIBULA PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083213
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2008
Days to Decision
60 days
Submission Type
Summary