510(k) K170888 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Renovis S141 Lumbar Interbody Fusion System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Aug 8, 2017 |
| Received | Mar 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170888
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.