ClearanceBrief
510(k) K201073 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Seaspine WaveForm C Interbody System

ApplicantSeaSpine Orthopedics Corporation, Carlsbad CA, US
DecisionSubstantially Equivalent, Sep 18, 2020
ReceivedApr 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K201073

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.