ClearanceBrief
510(k) K132493 ยท GDW Staple, Implantable

ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY

ApplicantCovidien, LLC, North Haven CT, US
DecisionSubstantially Equivalent, Oct 23, 2013
ReceivedAug 9, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K132493

DateFirm and productCodeLinked 510(k)
Sep 15, 2017Covidien LLC
Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally invasive general abdominal, gynecologic and thoracic
Terminated
GDWNone listed

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