ClearanceBrief
510(k) K070316 ยท MQP Spinal Vertebral Body Replacement Device

INTERPLATE VBR SYSTEM

ApplicantRsb Spine, LLC, Chesterland OH, US
DecisionSubstantially Equivalent, Apr 19, 2007
ReceivedFeb 1, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070316

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.