510(k) K183084 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Fuji Cervical Plate System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, May 29, 2019 |
| Received | Nov 6, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183084
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.