510(k) K133815 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
INTESS CERVICAL CAGE SYSTEM
| Applicant | Kalitec Direct, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Apr 16, 2014 |
| Received | Dec 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133815
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.