510(k) K211932 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Fixxsure Anterior Lumbar Plate and Screw System
| Applicant | Oak Tree Engineering, LLC, Huntington Beach CA, US |
| Decision | Substantially Equivalent, Jul 27, 2021 |
| Received | Jun 22, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211932
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.