510(k) K223671 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONDUIT LLIF Straight Inserters
| Applicant | Enztec Limited, Middleton, Christchurch, NZ |
| Decision | Substantially Equivalent, Jan 5, 2023 |
| Received | Dec 7, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223671
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.