510(k) K221844 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TDM Lumbar Interbody Fusion Cage System
| Applicant | Tdm Co., Ltd., Gwangju, KR |
| Decision | Substantially Equivalent, Aug 17, 2022 |
| Received | Jun 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221844
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.