510(k) K133911 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
GENESYS SPINE ANTERIOR BUTTRESS PLATE SYSTEM
| Applicant | Genesys Spine, Austin TX, US |
| Decision | Substantially Equivalent, Sep 3, 2014 |
| Received | Dec 23, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133911
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.