510(k) K191005 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ProLift® Expandable System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Jun 13, 2019 |
| Received | Apr 16, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191005
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.