Last synced on 18 April 2025 at 11:05 pm

SYNTHES LCP DISTAL TIBIA PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013248
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
82 days
Submission Type
Summary

SYNTHES LCP DISTAL TIBIA PLATES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013248
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
82 days
Submission Type
Summary