ClearanceBrief
510(k) K070224 ยท FTL Mesh, Surgical, Polymeric

ULTRAPRO PLUG

ApplicantETHICON, Inc., Somerville NJ, US
DecisionSubstantially Equivalent, Apr 17, 2007
ReceivedJan 24, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070224

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.