510(k) K133698 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNAPSE SYSTEM
| Applicant | Synthes USA Products, LLC, Raynham MA, US |
| Decision | Substantially Equivalent, Jan 16, 2014 |
| Received | Dec 3, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133698
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.