The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Excelsiusgps Spine 1.1 Interbody Module.
Device ID | K191100 |
510k Number | K191100 |
Device Name: | ExcelsiusGPS Spine 1.1 Interbody Module |
Classification | Orthopedic Stereotaxic Instrument |
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 | OLO |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-04-25 |
Decision Date | 2019-07-24 |
Summary: | summary |