510(k) K141897 ยท KWP Appliance, Fixation, Spinal Interlaminal
SYNAPSE SYSTEM, SYNTHES OC FUSION SYSTEM
| Applicant | Synthes USA Products, LLC, Raynham MA, US |
| Decision | Substantially Equivalent, Sep 25, 2014 |
| Received | Jul 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141897
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.