ClearanceBrief
510(k) K063491 ยท MQP Spinal Vertebral Body Replacement Device

T2 SCEPTOR SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Mar 5, 2007
ReceivedNov 17, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063491

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.