510(k) K120143 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL
| Applicant | Apollo Spine, Newbury NH, US |
| Decision | Substantially Equivalent, Feb 16, 2012 |
| Received | Jan 18, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120143
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.