ClearanceBrief
510(k) K142030 ยท MQP Spinal Vertebral Body Replacement Device

STGC-LORDOTIC

ApplicantCardinal Spine, LLC, San Diego CA, US
DecisionSubstantially Equivalent, Jan 23, 2015
ReceivedJul 25, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142030

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.