ClearanceBrief
510(k) K111626 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

ENDOSKELETON(R) TAS

ApplicantTitan Spine, LLC, Apple Valley MN, US
DecisionSubstantially Equivalent, Sep 9, 2011
ReceivedJun 10, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111626

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.