ClearanceBrief
510(k) K073161 ยท DZE Implant, Endosseous, Root-Form

REPLUS DENTAL IMPLANTS (HA)

ApplicantImplant Direct, LLC, Calabasas CA, US
DecisionSubstantially Equivalent, Mar 7, 2008
ReceivedNov 9, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073161

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.