ClearanceBrief
510(k) K020133 ยท DZE Implant, Endosseous, Root-Form

MODIFICATION TO THE MAESTRO SYSTEM

ApplicantBioHorizons Implant Systems, Inc., Birmingham AL, US
DecisionSubstantially Equivalent, Jan 25, 2002
ReceivedJan 15, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020133

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.