The following data is part of a premarket notification filed by Ingenium Spine with the FDA for Arisstos™ Spinal System.
Device ID | K173126 |
510k Number | K173126 |
Device Name: | Arisstos™ Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Ingenium Spine 3145 E. Chandler Blvd. #110 Phoenix, AZ 85048 |
Contact | David Brumfield |
Correspondent | Christine Scifert MRC-X, LLC 6075 Poplar Avenue, Suite 500 Memphis, TN 38119 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-29 |
Decision Date | 2017-12-05 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ARISSTOS 77836464 3920729 Live/Registered |
Showa Ika Kohgyo Co., Ltd. 2009-09-28 |