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 |