510(k) K062132 ยท MQP Spinal Vertebral Body Replacement Device
AVS PL PEEK SPACER SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 16, 2006 |
| Received | Jul 26, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062132
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.