ClearanceBrief
510(k) K081996 ยท FGE Stents, Drains And Dilators For The Biliary Ducts

FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM

ApplicantFlexible Stenting Solutions, Inc., Eatontown NJ, US
DecisionUnknown, Sep 15, 2009
ReceivedJul 14, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081996

DateFirm and productCodeLinked 510(k)
Jun 6, 2013Cordis Corporation
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for use in the palliation of malignant strictures in the biliary tree.
Terminated
FGENone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.