ClearanceBrief
510(k) K113539 ยท DZE Implant, Endosseous, Root-Form

REVOIS PRO IMPLANT STSYEM

ApplicantRiemser Arzneimittel AG, Greifswald-Insel Riems, DE
DecisionSubstantially Equivalent, May 3, 2013
ReceivedNov 30, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113539

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.