ClearanceBrief
510(k) K242267 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Gemini Medical Cage System

ApplicantZheJiang Decans Medical Devices Co., Ltd., Jiaxing, CN
DecisionSubstantially Equivalent, Oct 8, 2024
ReceivedAug 1, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242267

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.