ClearanceBrief
510(k) K243635 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

aprevo® anterior lumbar interbody fusion device with interfixation

ApplicantCarlsmed, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Dec 13, 2024
ReceivedNov 25, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K243635

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.