The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Xtend Anterior Cervical Plate System.
| Device ID | K092146 | 
| 510k Number | K092146 | 
| Device Name: | XTEND ANTERIOR CERVICAL PLATE SYSTEM | 
| Classification | Appliance, Fixation, Spinal Intervertebral Body | 
| Applicant | GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 | 
| Contact | Kelly J Baker | 
| Correspondent | Kelly J Baker GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403  | 
| Product Code | KWQ | 
| CFR Regulation Number | 888.3060 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2009-07-15 | 
| Decision Date | 2009-11-16 | 
| Summary: | summary |