510(k) K260015 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTERIS Thoracolumbar Plate System
| Applicant | SpineCraft, Westmont IL, US |
| Decision | Substantially Equivalent, Mar 4, 2026 |
| Received | Jan 5, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260015
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.