ClearanceBrief
510(k) K231371 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

BEE Cervical Cage

ApplicantNGMedical GmbH, Nonnweiler, DE
DecisionSubstantially Equivalent, Jan 12, 2024
ReceivedMay 12, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231371

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.