ClearanceBrief
510(k) K052061 ยท DZE Implant, Endosseous, Root-Form

MODUS IMF SCREWS 2.0

ApplicantMedartis, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 21, 2005
ReceivedJul 29, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052061

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.