ClearanceBrief
510(k) K120819 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

STALIF C

ApplicantCentinel Spine, Inc., West Chester PA, US
DecisionSubstantially Equivalent, Aug 31, 2012
ReceivedMar 19, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120819

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.