510(k) K172392 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lateral Spinal Truss System (LSTS) Interbody Fusion Device
| Applicant | 4Web, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Nov 7, 2017 |
| Received | Aug 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172392
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.