510(k) K083311 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Mar 4, 2009 |
| Received | Nov 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083311
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.