510(k) K180642 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Pro-Link® Ti Stand-Alone Cervical Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, May 10, 2018 |
| Received | Mar 12, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180642
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.