ClearanceBrief
510(k) K041722 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO VBR SPINAL SYSTEM

ApplicantDepuy Spine, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Sep 23, 2004
ReceivedJun 24, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K041722

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.