510(k) K113324 ยท KWP Appliance, Fixation, Spinal Interlaminal
REXIOUS HOOK FIXATION SYSTEMS
| Applicant | Dio Medical Co., Ltd., Brea CA, US |
| Decision | Substantially Equivalent, Mar 28, 2012 |
| Received | Nov 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113324
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.