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 |