ClearanceBrief
510(k) K972842 ยท LYC Bone Grafting Material, Synthetic

INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE

ApplicantInterpore Intl., Irvine CA, US
DecisionSubstantially Equivalent, Oct 30, 1997
ReceivedAug 1, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972842

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.