510(k) K202192 · KWQ Appliance, Fixation, Spinal Intervertebral Body
STRUXXURE®-L and STRUXXURE®-A Plate System
| Applicant | Nexxt Spine, LLC, Noblesville IN, US |
| Decision | Substantially Equivalent, Sep 17, 2020 |
| Received | Aug 5, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202192
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.