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SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111766
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/19/2011
Days to Decision
118 days
Submission Type
Summary

SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111766
510(k) Type
Traditional
Applicant
IDEV TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/19/2011
Days to Decision
118 days
Submission Type
Summary