510(k) K050861 ยท MQP Spinal Vertebral Body Replacement Device
PEEK CAS
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, May 27, 2005 |
| Received | Apr 5, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050861
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.