510(k) K061380 ยท MQP Spinal Vertebral Body Replacement Device
RETAIN RADIOLUCENT SPACER
| Applicant | Globus Medical, Inc., Phoenixville PA, US |
| Decision | Substantially Equivalent, Jun 8, 2006 |
| Received | May 18, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061380
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.