The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Si-lok Sacroiliac Joint Fixation System.
Device ID | K112028 |
510k Number | K112028 |
Device Name: | SI-LOK SACROILIAC JOINT FIXATION SYSTEM |
Classification | Screw, Fixation, Bone |
Applicant | GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 |
Contact | Wendy S Hills |
Correspondent | Wendy S Hills GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER 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 | 2011-07-15 |
Decision Date | 2011-12-09 |
Summary: | summary |