510(k) K203154 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
KASILOF Cervical Plate System
| Applicant | Kahtnu Surgical, Inc., Soldotna AK, US |
| Decision | Substantially Equivalent, Nov 5, 2020 |
| Received | Oct 22, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203154
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.