ClearanceBrief
510(k) K113738 ยท NHA Abutment, Implant, Dental, Endosseous

CREODENT SOLIDEX CUSTOM ABUTMENT

ApplicantCreodent Prosthetics, Ltd., New York NY, US
DecisionSubstantially Equivalent, Sep 17, 2013
ReceivedDec 20, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113738

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.