ClearanceBrief
510(k) K091946 ยท MQP Spinal Vertebral Body Replacement Device

VLIFT-S VERTEBRAL BODY REPLACEMENT SYSTEM, MODELS 488812XX, 488814XX, 488816XX, 488818XX

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Sep 25, 2009
ReceivedJun 30, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091946

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.