ClearanceBrief
510(k) K061151 ยท MQP Spinal Vertebral Body Replacement Device

PIONEER VERTEBRAL SPACER (VERTEBRAL SPACER)

ApplicantPioneer Surgical Technology, Marquette MI, US
DecisionSubstantially Equivalent, Jul 24, 2006
ReceivedApr 25, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061151

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.