The following data is part of a premarket notification filed by Zyga Technology, Inc. with the FDA for Simmetry Sacroiliac Joint Fusion System.
Device ID | K151818 |
510k Number | K151818 |
Device Name: | SImmetry Sacroiliac Joint Fusion System |
Classification | Sacroiliac Joint Fixation |
Applicant | Zyga Technology, Inc. 5600 Rowland Road, Suite 200 Minnetonka, MN 55343 |
Contact | Diane Brinza |
Correspondent | Diane Brinza Zyga Technology, Inc. 5600 Rowland Road, Suite 200 Minnetonka, MN 55343 |
Product Code | OUR |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-07-06 |
Decision Date | 2015-08-05 |
Summary: | summary |