ClearanceBrief
510(k) K062933 ยท MQP Spinal Vertebral Body Replacement Device

SYNTHES ORACLE SPACER

ApplicantSynthes Spine Co.Lp, West Chester PA, US
DecisionSubstantially Equivalent, Jan 31, 2007
ReceivedSep 28, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062933

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.