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 |