510(k) K211935 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ORIO-Ti Intervertebral Body Fusion Cage System
| Applicant | Spinecraft, LLC, Westmont IL, US |
| Decision | Substantially Equivalent, Sep 30, 2021 |
| Received | Jun 22, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211935
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.