510(k) K120063 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VENUS LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
| Applicant | L&K BIOMED Co., Ltd., Geumcheon-Gu, Seoul, KR |
| Decision | Substantially Equivalent, Apr 19, 2012 |
| Received | Jan 9, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120063
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.