ClearanceBrief
510(k) K011037 ยท MQP Spinal Vertebral Body Replacement Device

VERTEBRAL SPACER

ApplicantSynthes (Usa), Paoli PA, US
DecisionSubstantially Equivalent, Jul 1, 2002
ReceivedApr 5, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011037

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.