510(k) K132483 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
INNESIS PEEK CERVICAL CAGE
| Applicant | Bk Meditech, Co., Ltd., Stillwater MN, US |
| Decision | Substantially Equivalent, Apr 2, 2014 |
| Received | Aug 8, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132483
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.