510(k) K081730 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NOVEL CERVICAL SPINAL SPACER SYSTEM
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 19, 2008 |
| Received | Jun 18, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081730
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.