510(k) K082848 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NUBIC AND RABEA DEVICES
| Applicant | Signus Medizintechnik GmbH, Chesterland OH, US |
| Decision | Substantially Equivalent, Jul 24, 2009 |
| Received | Sep 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082848
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.