510(k) K113593 ยท KWP Appliance, Fixation, Spinal Interlaminal
NEXTGEN ALTIUS OCT SYSTEM
| Applicant | Biomet Spine (Aka Ebi, LLC), Parsippany NJ, US |
| Decision | Substantially Equivalent, Apr 17, 2012 |
| Received | Dec 5, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113593
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.