510(k) K180090 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Cure Lumbar Plate System
| Applicant | Meditech Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Apr 23, 2018 |
| Received | Jan 12, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180090
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.