510(k) K071372 ยท MQP Spinal Vertebral Body Replacement Device
MODIFICATION TO: INTERPLATE VBR SYSTEM
| Applicant | Rsb Spine, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Jun 11, 2007 |
| Received | May 16, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071372
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.