ClearanceBrief
510(k) K073067 ยท DZE Implant, Endosseous, Root-Form

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS

ApplicantDentsply International, Inc., York PA, US
DecisionSubstantially Equivalent, Feb 15, 2008
ReceivedOct 30, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073067

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.