Last synced on 30 May 2025 at 11:05 pm

SYNTHES TITANIUM DIASTAL FEMORAL NAIL (TI DFN) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970733
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1997
Days to Decision
33 days
Submission Type
Summary

SYNTHES TITANIUM DIASTAL FEMORAL NAIL (TI DFN) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970733
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1997
Days to Decision
33 days
Submission Type
Summary