510(k) K151819 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Integrity Spine Lumbar Interbody Fusion System
| Applicant | Integrity Spine Lumbar Interbody Fusion System, San Antonio TX, US |
| Decision | Substantially Equivalent, Nov 10, 2015 |
| Received | Jul 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151819
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.