510(k) K152355 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Twin Peaks Lumbar Interbody Fusion System
| Applicant | Spineway, Ecully, FR |
| Decision | Substantially Equivalent, Dec 10, 2015 |
| Received | Aug 20, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152355
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.