510(k) K192314 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
RESONATE Anterior Cervical Plate System
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Oct 23, 2019 |
| Received | Aug 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192314
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.