ClearanceBrief
510(k) K915733 ยท DZE Implant, Endosseous, Root-Form

STERI-OSS DRILLS AND TAPS

ApplicantSteri-Oss, Inc., Anaheim CA, US
DecisionSubstantially Equivalent, Jul 17, 1992
ReceivedDec 20, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915733

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.