510(k) K123909 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
AESCULAP CESPACE XP
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 15, 2013 |
| Received | Dec 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123909
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.