510(k) K020048 ยท MQP Spinal Vertebral Body Replacement Device
MODIFICATION TO GEO STRUCTURE
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 6, 2002 |
| Received | Jan 7, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020048
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.