510(k) K151408 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LOSPA IS Spinal System
| Applicant | Corentec Co., Ltd., Cheonan-Si, KR |
| Decision | Substantially Equivalent, Oct 2, 2015 |
| Received | May 26, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151408
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.