510(k) K180502 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
S128 Anterior Lumbar Interbody Fusion (ALIF) System
| Applicant | Renovis Surgical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Jun 14, 2018 |
| Received | Feb 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180502
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.