510(k) K172816 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TiGer Shark System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, Jan 26, 2018 |
| Received | Sep 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172816
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.