Last synced on 25 January 2026 at 3:41 am

OMNILINK. 018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060817
510(k) Type
Traditional
Applicant
Guidant Endovascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/15/2006
Days to Decision
80 days
Submission Type
Summary

OMNILINK. 018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060817
510(k) Type
Traditional
Applicant
Guidant Endovascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
6/15/2006
Days to Decision
80 days
Submission Type
Summary