510(k) K201024 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Expandable Titanium PLIF/TLIF System
| Applicant | Spectrum Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Apr 29, 2021 |
| Received | Apr 20, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201024
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.