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SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093893
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2010
Days to Decision
291 days
Submission Type
Summary

SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093893
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2010
Days to Decision
291 days
Submission Type
Summary