510(k) K140734 ยท KWP Appliance, Fixation, Spinal Interlaminal
NEXTGEN ALTIUS OCT SYSTEM
| Applicant | Ebi, LLC, Parsippany NJ, US |
| Decision | Substantially Equivalent, Dec 15, 2014 |
| Received | Mar 24, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140734
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.