Last synced on 25 April 2025 at 11:05 pm

SYNTHES 1.5MM TI BROW LIFT SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002935
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2000
Days to Decision
56 days
Submission Type
Summary

SYNTHES 1.5MM TI BROW LIFT SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002935
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2000
Days to Decision
56 days
Submission Type
Summary