ClearanceBrief
510(k) K040714 ยท DZE Implant, Endosseous, Root-Form

HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT

ApplicantInnova Corp., Washington DC, US
DecisionSubstantially Equivalent, Apr 9, 2004
ReceivedMar 18, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K040714

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.