510(k) K173885 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Genesys Spine Binary Lumbar Plate System
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Apr 3, 2018 |
| Received | Dec 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173885
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.