ClearanceBrief
510(k) K963897 ยท EMM Chisel, Osteotome, Surgical

STERI-OSS SINUS AUGMENTATION KIT

ApplicantSteri-Oss, Inc., Yorba Linda CA, US
DecisionSubstantially Equivalent, Nov 6, 1996
ReceivedSep 27, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963897

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.