ClearanceBrief
510(k) K043566 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO VERTE-STACK SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Jan 7, 2005
ReceivedDec 27, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K043566

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.