510(k) K041407 ยท MQP Spinal Vertebral Body Replacement Device
TITANIUM MESH IMPLANT
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Dec 29, 2004 |
| Received | May 27, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041407
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.