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 |