ClearanceBrief
510(k) K030249 ยท MQP Spinal Vertebral Body Replacement Device

SURGICAL TITANIUM MESH SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Feb 14, 2003
ReceivedJan 24, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030249

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.