ClearanceBrief
510(k) K210228 ยท ELE Implant, Subperiosteal

KLS Martin IPS Preprosthetic

ApplicantKLS-Martin L.P., Jacksonville FL, US
DecisionSubstantially Equivalent, Jul 8, 2022
ReceivedJan 28, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210228

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.