510(k) K231850 · NKG Posterior Cervical Screw System
QUARTEX® Occipito-Cervico-Thoracic Spinal System ExcelsiusGPS® Instruments
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Mar 14, 2024 |
| Received | Jun 23, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231850
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.