510(k) K232256 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Alcantara Thoracolumbar Plate System
| Applicant | Camber Spine Technologies, LLC, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Apr 16, 2024 |
| Received | Jul 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232256
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.