510(k) K173091 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Boundary Anterior Lumbar Buttress Plate
| Applicant | Nvision Biomedical Technologies, LLC, San Antonio TX, US |
| Decision | Substantially Equivalent, Dec 6, 2017 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173091
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.