510(k) K200958 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MODULIF-A Anterior Lumbar Interbody Fusion System
| Applicant | Spinal Stability, LLC, Austin TX, US |
| Decision | Substantially Equivalent, Aug 28, 2020 |
| Received | Apr 10, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200958
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.