510(k) K242771 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Tesera-k PL System and Tesera-k XL System
| Applicant | Kyocera Medical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Mar 20, 2025 |
| Received | Sep 13, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242771
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.