ClearanceBrief
510(k) K212498 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Stable-L Standalone Lumbar Interbody System

ApplicantNexus Spine, LLC, Salt Lake City UT, US
DecisionSubstantially Equivalent, Mar 18, 2022
ReceivedAug 9, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212498

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.