510(k) K241073 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DZ-Tabone Intervertebral Body Fusion Device
| Applicant | Shenzhen Dazhou Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 6, 2024 |
| Received | Apr 19, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241073
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.