510(k) K163670 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Rampart One Lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, May 8, 2017 |
| Received | Dec 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163670
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.