The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Coalition Agx Plate And Coalition Agx Spacer.
| Device ID | K142218 |
| 510k Number | K142218 |
| Device Name: | Coalition AGX Plate And Coalition AGX Spacer |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
| Contact | Kelly Baker |
| Correspondent | Kelly Baker GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
| Product Code | ODP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-08-12 |
| Decision Date | 2015-03-31 |
| Summary: | summary |