The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Modification To: Providence Anterior Cervical Plate System.
Device ID | K070775 |
510k Number | K070775 |
Device Name: | MODIFICATION TO: PROVIDENCE 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 | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-03-21 |
Decision Date | 2007-04-19 |
Summary: | summary |