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 |