510(k) K192076 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Binary® Anterior Cervical Plate System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Aug 29, 2019 |
| Received | Aug 2, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192076
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.