510(k) K060506 ยท MQP Spinal Vertebral Body Replacement Device
STRYKER SPINE VLIFT VERTEBRAL BODY REPLACEMENT SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, May 25, 2006 |
| Received | Feb 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060506
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.