ClearanceBrief
510(k) K843217 ยท DZE Implant, Endosseous, Root-Form

HOLLOW BASKET DENTAL IMPLANTS

ApplicantArtech Corp., Falls Church VA, US
DecisionSubstantially Equivalent, Oct 15, 1984
ReceivedAug 15, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843217

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.