ClearanceBrief
510(k) K953380 ยท DZE Implant, Endosseous, Root-Form

LABORATORY SUPPLIES

ApplicantSteri-Oss, Inc., Yorba Linda CA, US
DecisionSubstantially Equivalent, Sep 5, 1995
ReceivedJul 19, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953380

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.