510(k) K242517 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
ProAM ACDF System
| Applicant | Pro Surgical, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 20, 2024 |
| Received | Aug 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242517
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.