510(k) K232877 · MRW System, Facet Screw Spinal Device
FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C Stand Alone System
| Applicant | K&J Consulting Corporation, Lansdale PA, US |
| Decision | Substantially Equivalent, Dec 13, 2023 |
| Received | Sep 15, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232877
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.