ClearanceBrief
510(k) K090176 ยท MQP Spinal Vertebral Body Replacement Device

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Apr 27, 2009
ReceivedJan 23, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090176

DateFirm and productCodeLinked 510(k)
Dec 20, 2022NuVasive Inc
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Open, Classified
MQPNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.