510(k) K220449 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DePuy CONDUIT LLIF SQUID Inserter
| Applicant | Enztec Limited, Middleton, NZ |
| Decision | Substantially Equivalent, Jun 28, 2022 |
| Received | Feb 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220449
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.