ClearanceBrief
510(k) K023952 ยท DZE Implant, Endosseous, Root-Form

REPLACE ONE PIECE IMPLANT, HA, REPLACE ONE PIECE IMPLANT, TIUNITE

ApplicantNobel Biocare Uas, Inc., Yorba Linda, CA, US
DecisionSubstantially Equivalent, Jan 16, 2003
ReceivedNov 27, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023952

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.