ClearanceBrief
510(k) K083857 ยท MQP Spinal Vertebral Body Replacement Device

LDR SPINE ROI-C IMPLANT

ApplicantLdr Spine USA, Austin TX, US
DecisionSubstantially Equivalent, Feb 12, 2009
ReceivedDec 24, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083857

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.