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 |