ClearanceBrief
510(k) K040167 ยท MQP Spinal Vertebral Body Replacement Device

VERTE-STACK SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent for Some Indications, Feb 18, 2004
ReceivedJan 26, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K040167

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.