510(k) K132653 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NEOPLATE SPINE ANTERIOR FIXATION SYSTEM
| Applicant | Neoortho Productos Orthopedicos S/A, Aventura FL, US |
| Decision | Substantially Equivalent, May 14, 2014 |
| Received | Aug 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132653
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.