510(k) K183239 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CoreLink F3D Lateral System
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 19, 2018 |
| Received | Nov 20, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183239
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.