The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Corbel Spacers.
| Device ID | K201087 |
| 510k Number | K201087 |
| Device Name: | CORBEL Spacers |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | Globus Medical, Inc. Valley Forge Business Center 2560 General Armistead Ave. Audubon, PA 19403 |
| Contact | Jennifer Antonacci |
| Correspondent | Jennifer Antonacci Globus Medical, Inc. Valley Forge Business Center 2560 General Armistead Ave. Audubon, PA 19403 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-04-23 |
| Decision Date | 2020-07-31 |