510(k) K170318 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NeoFuse Ti3D PLIF/TLIF/Cervical Interbody
| Applicant | Ht Medical, LLC, Tulsa OK, US |
| Decision | Substantially Equivalent, Jul 12, 2017 |
| Received | Feb 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170318
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.