510(k) K111766 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS
| Applicant | Idev Technologies, Inc., Webster TX, US |
| Decision | Unknown, Oct 19, 2011 |
| Received | Jun 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111766
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 18, 2013 | IDEV Technologies, Inc. IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms Terminated |
FGE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.