ClearanceBrief
510(k) K233966 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Anterior Spine Truss System-Stand Alone (ASTS-SA)

Applicant4Web Medical, Inc., Frisco TX, US
DecisionSubstantially Equivalent, Apr 22, 2024
ReceivedDec 15, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233966

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.