The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Corridor Fixation System.
Device ID | K083442 |
510k Number | K083442 |
Device Name: | CORRIDOR FIXATION SYSTEM |
Classification | System, Facet Screw Spinal Device |
Applicant | GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 |
Contact | Kelly J Baker |
Correspondent | Kelly J Baker GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 |
Product Code | MRW |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-11-20 |
Decision Date | 2009-02-06 |
Summary: | summary |