510(k) K180990 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TirboLOX-L Lumbar IBFD
| Applicant | Captiva Spine, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Aug 13, 2018 |
| Received | Apr 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180990
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.