510(k) K162327 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
COUGAR® LS Lateral Cage System and COUGAR® System
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Dec 12, 2016 |
| Received | Aug 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162327
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.