510(k) K180814 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
CoreLink® M3 Stand-Alone Anterior Lumbar System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 10, 2018 |
| Received | Mar 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180814
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.