ClearanceBrief
510(k) K191489 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Genesys Spine 3DP Cervical Interbody System

ApplicantGenesys Spine, Austin TX, US
DecisionSubstantially Equivalent, Jan 8, 2020
ReceivedJun 4, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191489

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.