The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Assure Anterior Cervical Plate System.
Device ID | K040721 |
510k Number | K040721 |
Device Name: | ASSURE ANTERIOR CERVICAL PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | GLOBUS MEDICAL, INC. 303 SCHELL LANE Phoenixville, PA 19460 |
Contact | Kelly J Baker |
Correspondent | Kelly J Baker GLOBUS MEDICAL, INC. 303 SCHELL LANE Phoenixville, PA 19460 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-03-19 |
Decision Date | 2004-06-17 |
Summary: | summary |