Last synced on 16 May 2025 at 11:05 pm

4.0/2.5 MM SELF-DRILLING SCHANZ SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002605
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2000
Days to Decision
90 days
Submission Type
Summary

4.0/2.5 MM SELF-DRILLING SCHANZ SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002605
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2000
Days to Decision
90 days
Submission Type
Summary