510(k) K193106 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SpineFrontier Lumbar Interbody Fusion Device System
| Applicant | Spinefrontier, Inc., Malden MA, US |
| Decision | Substantially Equivalent, Jun 19, 2020 |
| Received | Nov 8, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193106
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.