510(k) K181655 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Renovis S180 Lateral Lumbar Interbody Fusion System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Sep 11, 2018 |
| Received | Jun 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181655
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.