510(k) K202380 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Born PT-LIF Cage HA
| Applicant | Spineworxx AG, St. Gallen, CH |
| Decision | Substantially Equivalent, Feb 19, 2021 |
| Received | Aug 20, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202380
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.