ClearanceBrief
510(k) K240416 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Tranquil-C Interbody System

ApplicantNexus Spine, LLC, Salt Lake City UT, US
DecisionSubstantially Equivalent, Mar 12, 2024
ReceivedFeb 12, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K240416

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.