510(k) K201453 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Fortilink Cages with TiPlus Technology
| Applicant | Paradigm Spine GmbH, New York NY, US |
| Decision | Substantially Equivalent, Oct 7, 2020 |
| Received | Jun 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201453
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.