510(k) K173182 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ProLift® Expandable System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Dec 20, 2017 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173182
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.