510(k) K170395 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Talos® Lumbar (HA) PEEK IBF Devices
| Applicant | Meditech Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Jun 2, 2017 |
| Received | Feb 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170395
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.