510(k) K242457 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EARP Interbody System
| Applicant | Retropsoas Technologies, LLC, Frontenac MO, US |
| Decision | Substantially Equivalent, Oct 7, 2024 |
| Received | Aug 19, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242457
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.