510(k) K173432 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ENZA-A Titanium ALIF
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, Apr 18, 2018 |
| Received | Nov 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173432
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.