ClearanceBrief
510(k) K182477 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Cervical Spacer

ApplicantAdditive Implants, LLC, Pheonix AZ, US
DecisionSubstantially Equivalent, Jan 28, 2019
ReceivedSep 10, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182477

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.