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 |