The following data is part of a premarket notification filed by Integrity Implants, Inc with the FDA for Linesider™ Spinal System.
| Device ID | K190360 |
| 510k Number | K190360 |
| Device Name: | LineSider™ Spinal System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Integrity Implants, Inc 850 Parkway Street Jupiter, FL 33477 |
| Contact | Lauren Kamer |
| Correspondent | Meredith Lee May Empirical Consulting LLC 4628 Northpark Drive Colorado Springs, CO 80918 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-02-15 |
| Decision Date | 2019-06-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LINESIDER 87157129 not registered Live/Pending |
Integrity Implants Inc. 2016-08-31 |
![]() LINESIDER 75545086 2380446 Dead/Cancelled |
Soares, Charles L. 1998-08-31 |
![]() LINESIDER 75545086 2380446 Dead/Cancelled |
Soares, Lola 1998-08-31 |