Last synced on 25 January 2026 at 3:41 am

SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050606
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2005
Days to Decision
27 days
Submission Type
Summary

SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050606
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2005
Days to Decision
27 days
Submission Type
Summary