510(k) K032371 ยท MQP Spinal Vertebral Body Replacement Device
TITANIUM MESH SYSTEM
| Applicant | Encore Medical L.P., Austin TX, US |
| Decision | Substantially Equivalent, Feb 12, 2004 |
| Received | Aug 1, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032371
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.