510(k) K241992 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Catalyft LS Expandable Interbody System
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Oct 28, 2024 |
| Received | Jul 8, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241992
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.