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MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003336
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/22/2000
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003336
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/22/2000
Days to Decision
28 days
Submission Type
Summary