ClearanceBrief
510(k) K152568 ยท PLR Spinal Vertebral Body Replacement Device - Cervical

C-VBR

ApplicantCardinal Spine, LLC, Louisville KY, US
DecisionSubstantially Equivalent, Feb 11, 2016
ReceivedSep 9, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152568

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.