ClearanceBrief
510(k) K040928 ยท MQP Spinal Vertebral Body Replacement Device

EXPANDABLE PEEK VBR IMPLANT

ApplicantInterpore Cross Intl., Irvine CA, US
DecisionSubstantially Equivalent, Aug 27, 2004
ReceivedApr 9, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040928

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.