510(k) K141791 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
BIOMET FUSION SYSTEM
| Applicant | Biomet Spine, Broomfield CO, US |
| Decision | Substantially Equivalent, Oct 9, 2014 |
| Received | Jul 2, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141791
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.