510(k) K171468 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FUSE Spinal System
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Jun 13, 2017 |
| Received | May 18, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171468
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.