510(k) K110783 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VENUS INTERBODY FIXATION SYSTEM- VENUS PLIF/TLIF, ALIF PEEK CAGE
| Applicant | L&K BIOMED Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Oct 24, 2011 |
| Received | Mar 21, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110783
No recall in the FDA data names this 510(k).
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