510(k) K121733 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INFILL INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Pinnacle Spine Group, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Jul 13, 2012 |
| Received | Jun 13, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121733
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.