ClearanceBrief
510(k) K111469 ยท MQP Spinal Vertebral Body Replacement Device

STAXXSD SYSTEM

ApplicantSpine Wave, Inc., Shelton CT, US
DecisionSubstantially Equivalent, Jul 19, 2011
ReceivedMay 27, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K111469

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.