510(k) K180556 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Corelink Foundation 3D Anterior Lumbar System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Jul 27, 2018 |
| Received | Mar 1, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180556
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.