510(k) K142589 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS, Endoskeleton TAS, Endoskeleton TC, Endoskeleton TL
| Applicant | Titan Spine, LLC, Mequon WI, US |
| Decision | Substantially Equivalent, Oct 17, 2014 |
| Received | Sep 15, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142589
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.