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MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031777
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/7/2003
Days to Decision
27 days
Submission Type
Summary

MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031777
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/7/2003
Days to Decision
27 days
Submission Type
Summary