510(k) K211474 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Kleiner KG2 System
| Applicant | BAAT Medical Products B.V., Hengelo, NL |
| Decision | Substantially Equivalent, Sep 14, 2021 |
| Received | May 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211474
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.