510(k) K183071 ยท PLR Spinal Vertebral Body Replacement Device - Cervical
VLIFT-s Vertebral Body Replacement System
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Jan 10, 2019 |
| Received | Nov 5, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183071
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.