510(k) K131533 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CAYMAN MI PLATE SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Nov 9, 2013 |
| Received | May 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131533
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.