The following data is part of a premarket notification filed by Integrity Implants Inc. with the FDA for Linesider™ Spinal System.
Device ID | K203367 |
510k Number | K203367 |
Device Name: | LineSider™ Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Integrity Implants Inc. 354 Hiatt Drive Palm Beach Gardens, FL 33418 |
Contact | Lauren Kamer |
Correspondent | Nathan Wright Empirical Testing Corp. 4628 Northpark Drive Colorado Springs, CO 80918 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-11-16 |
Decision Date | 2020-12-03 |
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 |