510(k) K153250 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Mar 16, 2016 |
| Received | Nov 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153250
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.