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 |