ClearanceBrief
510(k) K142016 ยท MQP Spinal Vertebral Body Replacement Device

CAPRI

ApplicantK2m, Inc., Leesburg VA, US
DecisionSubstantially Equivalent, Nov 6, 2014
ReceivedJul 25, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142016

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.