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 |