510(k) K220453 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FlareHawk Interbody Fusion System
| Applicant | Integrity Implants, Inc., Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Mar 24, 2022 |
| Received | Feb 17, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220453
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.