510(k) K190584 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CAYMAN LP Plate System
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, May 15, 2019 |
| Received | Mar 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190584
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.