The following data is part of a premarket notification filed by Coorstek Medical with the FDA for Integrity-si Tm Fusion System.
| Device ID | K161755 |
| 510k Number | K161755 |
| Device Name: | Integrity-SI TM Fusion System |
| Classification | Sacroiliac Joint Fixation |
| Applicant | CoorsTek Medical 560 W. GOLF COURSE RD. Providence, UT 84332 |
| Contact | Steve Brown |
| Correspondent | Steve Brown CoorsTek Medical 560 WEST GOLF COURSE ROAD. Providence, UT 84332 |
| Product Code | OUR |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-06-27 |
| Decision Date | 2016-12-14 |
| Summary: | summary |