ClearanceBrief
510(k) K023237 ยท FTM Mesh, Surgical

XYLOS SURGICAL MESH

ApplicantXylos Corporation, Washington DC, US
DecisionSubstantially Equivalent, Mar 18, 2003
ReceivedSep 27, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023237

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.