ClearanceBrief
510(k) K131705 ยท GDW Staple, Implantable

ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY

ApplicantCovidien, Formerly US Surgical A Divison of Tyco H, North Haven CT, US
DecisionSubstantially Equivalent, Jul 1, 2013
ReceivedJun 11, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K131705

No recall in the FDA data names this 510(k).

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