510(k) K211388 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lateral Spine Truss System (LSTS) Interbody Fusion Device
| Applicant | 4Web Medical, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Aug 5, 2021 |
| Received | May 5, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211388
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.