510(k) K180215 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
DYNA-LINK ELITE Stand-Alone Anterior Lumbar System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Sep 13, 2018 |
| Received | Jan 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180215
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.