510(k) K063139 ยท NVR Intervertebral Fusion Device With Bone Graft, Solid-Sphere, Lumbar
SPINAL STABILIZING SPHERE SYSTEM
| Applicant | Biomet Spine, Warsaw IN, US |
| Decision | Unknown, Apr 4, 2007 |
| Received | Oct 16, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063139
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.