510(k) K150521 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Interbody Fusion (IBF)/Vertebral Body Replacement(VBR) System
| Applicant | Rti Surgical, Inc. Dba Rti Biologics, Alachua FL, US |
| Decision | Substantially Equivalent, May 15, 2015 |
| Received | Mar 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150521
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.