ClearanceBrief
510(k) K843557 ยท ELE Implant, Subperiosteal

K-APATITE 20-40 MESH K-APATITE 40-60

ApplicantKatecho, Inc., Des Moines IA, US
DecisionSubstantially Equivalent, Nov 30, 1984
ReceivedSep 10, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843557

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.