ClearanceBrief
510(k) K170074 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

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ApplicantNvision Biomedical Technologies, LLC, San Antonio TX, US
DecisionSubstantially Equivalent, Jan 24, 2017
ReceivedJan 9, 2017
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K170074

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.