510(k) K231704 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Oct 19, 2023 |
| Received | Jun 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231704
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.