ClearanceBrief
510(k) K061401 ยท MQP Spinal Vertebral Body Replacement Device

INTERPLATE VBR SYSTEM

ApplicantRsb Spine, LLC, Chesterland OH, US
DecisionSubstantially Equivalent, Aug 18, 2006
ReceivedMay 19, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061401

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.