510(k) K072537 ยท MQP Spinal Vertebral Body Replacement Device
CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM
| Applicant | Creaspine Sas, North Attleboro MA, US |
| Decision | Substantially Equivalent, Dec 18, 2007 |
| Received | Sep 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072537
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.