510(k) K221490 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tritanium C Anterior Cervical Cage, Tritanium PL Cage, Tritanium TL Curved Posterior Lumbar Cage, Tritanium X PL Expandable Posterior Lumbar Cage, Tritanium X TL Expandable Curved Posterior Lumbar Cage, Stryker Spine VLIFT Vertebral Body Replacement System, VLIFT-s Vertebral Body Replacement System,
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Feb 14, 2023 |
| Received | May 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221490
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.