510(k) K151934 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
ROI-C Titanium-Coated Implant System
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Dec 7, 2015 |
| Received | Jul 14, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151934
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.