510(k) K221719 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ABTross ALIF Expandable Cage System
| Applicant | Aegis Spine, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Nov 3, 2022 |
| Received | Jun 13, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221719
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.