ClearanceBrief
510(k) K172323 ยท MQP Spinal Vertebral Body Replacement Device

Omnia Medical VBR

ApplicantOmnia Medical, LLC, Morgantown WV, US
DecisionSubstantially Equivalent, Oct 26, 2017
ReceivedAug 1, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172323

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.