510(k) K191834 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Stand-Alone ALIF Titanium System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Dec 16, 2019 |
| Received | Jul 9, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191834
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.