ClearanceBrief
510(k) K130317 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

GENESYS SPINE APACHE IBFD STAR CERVICAL SYSTEM

ApplicantGenesys Spine, Austin TX, US
DecisionSubstantially Equivalent, Dec 11, 2013
ReceivedFeb 8, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130317

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.