510(k) K050624 ยท MQP Spinal Vertebral Body Replacement Device
STRYKER SPINE AVS PL PEEK SPACER
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 11, 2005 |
| Received | Mar 11, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050624
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.