510(k) K142504 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SpineFrontier Lumbar Interbody Fusion Device System
| Applicant | Spinefrontier, Inc., Beverly MA, US |
| Decision | Substantially Equivalent, May 13, 2015 |
| Received | Sep 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142504
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.