ClearanceBrief
510(k) K120414 ยท DZE Implant, Endosseous, Root-Form

OSSEOSPEED PLUS

ApplicantAstra Tech AB, San Diego CA, US
DecisionSubstantially Equivalent, Jul 31, 2012
ReceivedFeb 10, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120414

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.