ClearanceBrief
510(k) K010530 ยท MQP Spinal Vertebral Body Replacement Device

GEO STRUCTURE

ApplicantInterpore Cross Intl., Irvine CA, US
DecisionSubstantially Equivalent, Aug 3, 2001
ReceivedFeb 23, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010530

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.