510(k) K181625 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Life Spine Resolute Threaded Cage System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Dec 11, 2018 |
| Received | Jun 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181625
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.