ClearanceBrief
510(k) K024049 ยท MQP Spinal Vertebral Body Replacement Device

VERTE-SPAN SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Feb 26, 2003
ReceivedDec 9, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K024049

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.