ClearanceBrief
510(k) K042201 ยท MQP Spinal Vertebral Body Replacement Device

NOVEL VBR SPINAL SYSTEM

ApplicantAlphatec/Nexmed, Carlsbad CA, US
DecisionSubstantially Equivalent, Oct 7, 2004
ReceivedAug 13, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042201

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.