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 |