Last synced on 6 June 2025 at 11:06 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
K073460
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2008
Days to Decision
73 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
K073460
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2008
Days to Decision
73 days
Submission Type
Summary