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 |