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MODIFICATION TO PRECISE NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012993
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2001
Days to Decision
29 days
Submission Type
Summary

MODIFICATION TO PRECISE NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012993
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2001
Days to Decision
29 days
Submission Type
Summary