510(k) K192678 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Genesys Spine Binary® Lumbar Plate System
| Applicant | Genesys Spine, Austin Tx, US |
| Decision | Substantially Equivalent, Oct 24, 2019 |
| Received | Sep 26, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192678
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.