510(k) K170643 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System
| Applicant | Rti Surgical, Inc. Dba Rti Biologics, Alachua FL, US |
| Decision | Substantially Equivalent, Apr 14, 2017 |
| Received | Mar 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170643
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.