510(k) K161223 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
TransContinental® M Spacers and InterContinental® Plate-Spacers
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jul 15, 2016 |
| Received | Apr 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161223
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.