The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Creo Stabilization System, Navigation Instruments, Excelsiusgps Instruments.
| Device ID | K191835 | 
| 510k Number | K191835 | 
| Device Name: | CREO Stabilization System, Navigation Instruments, ExcelsiusGPS Instruments | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| 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 | NKB | 
| Subsequent Product Code | HAW | 
| Subsequent Product Code | KWP | 
| Subsequent Product Code | OLO | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2019-07-09 | 
| Decision Date | 2019-08-06 |