ClearanceBrief
510(k) K061752 ยท MQP Spinal Vertebral Body Replacement Device

SPINAL USA VBR SYSTEM

ApplicantSpinal USA, Flowood MS, US
DecisionSubstantially Equivalent, Aug 15, 2006
ReceivedJun 21, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061752

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.