510(k) K080302 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CAYMAN BUTTRESS PLATE SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Mar 24, 2008 |
| Received | Feb 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080302
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.