510(k) K181231 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DePuy Synthes T-PAL Spacer System
| Applicant | Depuy Synthes Spine, Raynham MA, US |
| Decision | Substantially Equivalent, Dec 6, 2018 |
| Received | May 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181231
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.