ClearanceBrief
510(k) K043479 ยท MQP Spinal Vertebral Body Replacement Device

MC+ PARTIAL VBR

ApplicantLdr Spine USA, Austin TX, US
DecisionSubstantially Equivalent, Jun 30, 2005
ReceivedDec 16, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043479

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.