510(k) K200613 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Tritanium® X TL Expandable Curved Posterior Lumbar Cage
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 15, 2020 |
| Received | Mar 9, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200613
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.