510(k) K153436 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LATERAL Spine Truss System
| Applicant | 4Web, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Jun 6, 2016 |
| Received | Nov 27, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153436
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.