510(k) K073351 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CRYSTAL
| Applicant | Spinal Elements, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jan 24, 2008 |
| Received | Nov 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073351
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.