510(k) K190544 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
XIHPOS ZFUZE Interbody Fusion System
| Applicant | Difusion Technologies, Austin TX, US |
| Decision | Substantially Equivalent, Nov 1, 2019 |
| Received | Mar 4, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190544
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.