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MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063481
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/14/2007
Days to Decision
301 days
Submission Type
Summary

MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063481
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
9/14/2007
Days to Decision
301 days
Submission Type
Summary