510(k) K031302 ยท MQP Spinal Vertebral Body Replacement Device
SUSTAIN SPACER
| Applicant | Globus Medical, Inc., Phoenixville PA, US |
| Decision | Substantially Equivalent, Jun 27, 2003 |
| Received | Apr 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031302
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.