510(k) K223065 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices
| Applicant | Adcura, Inc., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Oct 26, 2022 |
| Received | Sep 30, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223065
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.