510(k) K212823 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DePuy CONDUIT LLIF Angled Inserters
| Applicant | Enztec Limited, Middleton, NZ |
| Decision | Substantially Equivalent, Nov 1, 2021 |
| Received | Sep 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212823
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.