ClearanceBrief
510(k) K002188 ยท DZE Implant, Endosseous, Root-Form

SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8D,

ApplicantCore-Vent Corp., Las Vegas NV, US
DecisionSubstantially Equivalent, Oct 30, 2000
ReceivedJul 20, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002188

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.