ClearanceBrief
510(k) K010930 ยท MQP Spinal Vertebral Body Replacement Device

LIFT VB SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Oct 24, 2001
ReceivedMar 28, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010930

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.