ClearanceBrief
510(k) K051000 ยท MQP Spinal Vertebral Body Replacement Device

FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE

ApplicantSpinal Concepts, Inc., Austin TX, US
DecisionSubstantially Equivalent, May 19, 2005
ReceivedApr 20, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K051000

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.