510(k) K240126 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ProAM ALIF System
| Applicant | Pro Surgical, Inc., Encinitas CA, US |
| Decision | Substantially Equivalent, May 3, 2024 |
| Received | Jan 16, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240126
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.