510(k) K213355 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Toro-L Interbody Fusion System
| Applicant | Integrity Implants, Inc., Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Mar 25, 2022 |
| Received | Oct 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213355
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.