ClearanceBrief
510(k) K230731 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Zavation ALIF System

ApplicantZavation Medical Products, LLC, Flowood MS, US
DecisionSubstantially Equivalent, Jun 14, 2023
ReceivedMar 16, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230731

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.