510(k) K153400 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ProLift Expandable System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Mar 7, 2016 |
| Received | Nov 24, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153400
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.