510(k) K070381 ยท MQP Spinal Vertebral Body Replacement Device
THEKEN VU MESH VBR SYSTEM
| Applicant | Theken Spine, LLC, Akron OH, US |
| Decision | Substantially Equivalent, Apr 25, 2007 |
| Received | Feb 8, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070381
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.