ClearanceBrief
510(k) K062073 ยท MQP Spinal Vertebral Body Replacement Device

VERTE-STACK SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Aug 14, 2006
ReceivedJul 21, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062073

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.