The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Anthem® Fracture System.
| Device ID | K213591 | 
| 510k Number | K213591 | 
| Device Name: | ANTHEM® Fracture System | 
| Classification | Plate, Fixation, Bone | 
| Applicant | Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 | 
| Contact | Jennifer Antonacci | 
| Correspondent | Jennifer Antonacci Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403  | 
| Product Code | HRS | 
| Subsequent Product Code | HTN | 
| Subsequent Product Code | HWC | 
| CFR Regulation Number | 888.3030 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2021-11-12 | 
| Decision Date | 2022-01-26 |