The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Captivate® Compression Screws.
| Device ID | K222409 |
| 510k Number | K222409 |
| Device Name: | CAPTIVATE® Compression Screws |
| Classification | Screw, Fixation, Bone |
| 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 | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-08-10 |
| Decision Date | 2022-09-08 |