510(k) K060762 ยท MQP Spinal Vertebral Body Replacement Device
AESCULAP PEEK VERTEBRAL BODY REPLACEMENT SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Sep 14, 2006 |
| Received | Mar 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060762
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.