510(k) K171495 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Zyston Strut Open Titanium Spacer System
| Applicant | Zimmer Biomet Spine, Inc., Westminister CO, US |
| Decision | Substantially Equivalent, Feb 12, 2018 |
| Received | May 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171495
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.