510(k) K252113 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PRADO Lumbar Interbody Fusion System
| Applicant | Bethesda Medical Devices, Brunswick OH, US |
| Decision | Substantially Equivalent, Aug 5, 2025 |
| Received | Jul 7, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K252113
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.