ClearanceBrief
510(k) K210470 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

C-CURVE Interbody Fusion Device

ApplicantMedicrea International SA, Rillieux-La-Pape, FR
DecisionSubstantially Equivalent, Sep 3, 2021
ReceivedFeb 17, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210470

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.