Last synced on 4 February 2023 at 10:33 pm

MODIFICATION TO:SYNTHES (USA) TITANIUM WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042606
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
245 days
Submission Type
Summary

MODIFICATION TO:SYNTHES (USA) TITANIUM WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042606
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
245 days
Submission Type
Summary