ClearanceBrief
510(k) K122622 ยท MQP Spinal Vertebral Body Replacement Device

ENDURAMESH

ApplicantLucero Medical, LLC, Avon Lake OH, US
DecisionSubstantially Equivalent, Sep 19, 2012
ReceivedAug 28, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K122622

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.