510(k) K182007 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Dec 7, 2018 |
| Received | Jul 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182007
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.