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OMNILINK. 018 BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
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)
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