510(k) K150206 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
InFill Interbody Fusion Devices
| Applicant | Pinnacle Spine Group, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Apr 3, 2015 |
| Received | Jan 29, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150206
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.