510(k) K191367 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Harrier-SA Lumbar Interbody System
| Applicant | Choice Spine, LLC, Knoxville TN, US |
| Decision | Substantially Equivalent, Jul 5, 2019 |
| Received | May 22, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191367
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.