ClearanceBrief
510(k) K033483 ยท DZE Implant, Endosseous, Root-Form

KLS-MARTIN ORTHO ANCHORAGE SYSTEM

ApplicantKLS-Martin L.P., Jacksonville FL, US
DecisionSubstantially Equivalent, Jan 15, 2004
ReceivedNov 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033483

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.