ClearanceBrief
510(k) K183054 ยท MQP Spinal Vertebral Body Replacement Device

SYNMESH System

ApplicantDepuy Synthes Spine, Raynham MA, US
DecisionSubstantially Equivalent, May 23, 2019
ReceivedNov 2, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183054

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.