510(k) K160066 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Pro-Link® Stand-Alone Cervical Spacer System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Sep 2, 2016 |
| Received | Jan 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160066
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.