The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Fortify(tm) And Fortify(tm)-r Corpectomy Spacers.
Device ID | K112756 |
510k Number | K112756 |
Device Name: | FORTIFY(TM) AND FORTIFY(TM)-R CORPECTOMY SPACERS |
Classification | Spinal Vertebral Body Replacement Device |
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 | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-09-21 |
Decision Date | 2011-10-07 |
Summary: | summary |