ClearanceBrief
510(k) K172408 ยท LOD Bone Cement

Biomet Bone Cement R

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Oct 5, 2017
ReceivedAug 9, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172408

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.