510(k) K142345 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Talos-C(HA) Cervical Intervertebral Body Fusion Devices
| Applicant | Meditech Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Feb 22, 2015 |
| Received | Aug 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142345
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.