ClearanceBrief
510(k) K142645 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Avenue T TLIF Cage

ApplicantLdr Spine USA, Inc., Austin TX, US
DecisionSubstantially Equivalent, Jun 11, 2015
ReceivedSep 17, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142645

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.