ClearanceBrief
510(k) K013382 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO: STACKABLE CAGE SYSTEM

ApplicantDepuyacromed, Raynham MA, US
DecisionSubstantially Equivalent, Nov 7, 2001
ReceivedOct 12, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K013382

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.