The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Colosseum Mesh.
Device ID | K190147 |
510k Number | K190147 |
Device Name: | COLOSSEUM Mesh |
Classification | Spinal Vertebral Body Replacement Device |
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 | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-01-29 |
Decision Date | 2019-05-08 |