510(k) K232014 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONDUIT ATP Inserters
| Applicant | Enztec Limited, Christchurch, NZ |
| Decision | Substantially Equivalent, Sep 1, 2023 |
| Received | Jul 6, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232014
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.