510(k) K113170 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CERVICAL PLATE
| Applicant | Eisertech, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Apr 6, 2012 |
| Received | Oct 27, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113170
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.