ClearanceBrief
510(k) K081194 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)

ApplicantRsb Spine, LLC, Chesterland OH, US
DecisionSubstantially Equivalent, May 29, 2008
ReceivedApr 28, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081194

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.