The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Captivate™ Compression Screws.
| Device ID | K162825 |
| 510k Number | K162825 |
| Device Name: | CAPTIVATE™ Compression Screws |
| Classification | Screw, Fixation, Bone |
| 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 | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-10-07 |
| Decision Date | 2017-05-01 |
| Summary: | summary |