510(k) K171351 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Posterior Spine Truss System (PSTS) Interbody Fusion Device
| Applicant | 4Web, Inc., Frisco TX, US |
| Decision | Substantially Equivalent, Sep 8, 2017 |
| Received | May 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171351
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.