The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Resonate Anterior Cervical Plate System.
Device ID | K192314 |
510k Number | K192314 |
Device Name: | RESONATE Anterior Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 |
Contact | Kelly J Baker |
Correspondent | Kelly J Baker Globus Medical Inc. 2560 General Armistead Ave. 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 | 2019-08-26 |
Decision Date | 2019-10-23 |
Summary: | summary |