ClearanceBrief
510(k) K123045 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

BRIGADE STANDALONE SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Apr 16, 2013
ReceivedOct 1, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K123045

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.