510(k) K143450 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Ackermann Intervertebral Body Fusion Device
| Applicant | Ackermann Instrumente GmbH, Rietheim, Weilheim, DE |
| Decision | Substantially Equivalent, Sep 16, 2015 |
| Received | Dec 2, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143450
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.