510(k) K022143 ยท MQP Spinal Vertebral Body Replacement Device
INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 23, 2003 |
| Received | Jul 2, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022143
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.