510(k) K150788 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral Body Fusion Devices, Talos -C(HA) Cervical Intervertebral Body Fusion Devices
| Applicant | Meditech Spine, LLC, Atlanta GA, US |
| Decision | Substantially Equivalent, Oct 14, 2015 |
| Received | Mar 25, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150788
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.