510(k) K233735 · KWQ Appliance, Fixation, Spinal Intervertebral Body
ADIRA Lateral Plate System
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jan 25, 2024 |
| Received | Nov 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233735
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.