510(k) K171538 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Cure Lumbar Plate System
| Applicant | Meditech Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Jun 16, 2017 |
| Received | May 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171538
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.