510(k) K170399 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Endoskeleton TO Interbody Fusion Device (IBD)
| Applicant | Titan Spine, LLC, Mequon WI, US |
| Decision | Substantially Equivalent, Jul 6, 2017 |
| Received | Feb 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170399
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.