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OMNILINK. 018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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