510(k) K120840 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
LEXUS CERVICAL INTERVERTEBRAL BODY FUSION CAGE SYSTEM
| Applicant | L&K BIOMED Co., Ltd., Geumcheon-Gu, Seoul, KR |
| Decision | Substantially Equivalent, May 24, 2012 |
| Received | Mar 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120840
No recall in the FDA data names this 510(k).
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