ClearanceBrief
510(k) K031635 ยท MQP Spinal Vertebral Body Replacement Device

DEPUY ACROMED VBR SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Jun 23, 2003
ReceivedMay 27, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031635

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.