ClearanceBrief
510(k) K121982 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

SOVEREIGN SPINAL SYSTEM

ApplicantMedtronic Sofamor Danek, Memphis TN, US
DecisionSubstantially Equivalent, Jul 26, 2012
ReceivedJul 6, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121982

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.