The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Fortify Integrated Corpectomy Spacers, (fortify I And Fortify I-r).
Device ID | K121107 |
510k Number | K121107 |
Device Name: | FORTIFY INTEGRATED CORPECTOMY SPACERS, (FORTIFY I AND FORTIFY I-R) |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
Contact | Sarah M Fitzgerald |
Correspondent | Sarah M Fitzgerald GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-04-12 |
Decision Date | 2012-07-03 |
Summary: | summary |