ClearanceBrief
510(k) K080572 ยท MQP Spinal Vertebral Body Replacement Device

LDR SPINE ROI-A IMPLANT

ApplicantLdr Spine USA, Austin TX, US
DecisionSubstantially Equivalent, Apr 7, 2008
ReceivedFeb 29, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080572

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.