510(k) K152193 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Renovis Anterior Cervical Plate System
| Applicant | Renovis Surgical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Sep 25, 2015 |
| Received | Aug 5, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152193
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.