510(k) K151483 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Biomet Spine Fusion System
| Applicant | Biomet Spine, LLC, Broomfield CO, US |
| Decision | Substantially Equivalent, Jul 31, 2015 |
| Received | Jun 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151483
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.