510(k) K181096 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Avenue P Cage System
| Applicant | Zimmer Biomet Spine, Inc., Westminister CO, US |
| Decision | Substantially Equivalent, Jan 15, 2019 |
| Received | Apr 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181096
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.