ClearanceBrief
510(k) K082748 ยท FTL Mesh, Surgical, Polymeric

ATRIUM PROLITE S MESH

ApplicantAtrium Medical Corp., Hudson NH, US
DecisionSubstantially Equivalent, Jan 14, 2009
ReceivedSep 19, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082748

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.