ClearanceBrief
510(k) K130547 ยท FTM Mesh, Surgical

ENDOFORM RECONSTRUCTIVE TEMPLATE

ApplicantMesynthe, Ltd., San Diego CA, US
DecisionSubstantially Equivalent, May 31, 2013
ReceivedMar 4, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130547

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.