510(k) K202820 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Australis Anterior Lumbar Cage System
| Applicant | Prism Surgical Designs Pty, Ltd., Milton, AU |
| Decision | Substantially Equivalent, Dec 22, 2020 |
| Received | Sep 24, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202820
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.