LineSider Spinal System
FDA 510(k) K190360 · Integrity Implants, Inc.
510(k) numberK190360
Submission
- Device name
- LineSider Spinal System
- Applicant
- Integrity Implants, Inc.
Jupiter, FL, US - Received
- February 15, 2019
- Decision date
- June 21, 2019
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- NKB – Thoracolumbosacral Pedicle Screw System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3070
- Specialty
- Orthopedic
- Implant
- Yes
Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.
Other 510(k)s with product code NKB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262828 | KHEIRON® Spinal Fixation System, including patient specific K-RODNKB · Special | S.M.A.I.O | 09/04/2026SE |
| K260362 | QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS…NKB · Traditional | MANTIZ Co., Ltd. | 07/24/2026SE |
| K253943 | Tiger 2 SystemNKB · Traditional | Zavation Medical Products, LLC | 07/24/2026SE |
| K261284 | Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemNKB · Traditional | Alphatec Spine, Inc. | 07/14/2026SE |
| K253802 | KHEIRON® Spinal Fixation System, including patient specific K-RODNKB · Special | S.M.A.I.O | 07/01/2026SE |
| K253045 | Socko Vimax Spinal Fixation SystemNKB · Traditional | Socko Medical Co., Ltd. | 06/17/2026SE |
| K251251 | ChanPin Pedicle Screw Spinal SystemNKB · Traditional | Chanpin Medtak Co., Ltd. | 06/09/2026SE |
| K260989 | Varion Thoracolumbar Fixation SystemNKB · Traditional | Kyocera Medical Technologies Inc. (KMTI) | 05/15/2026SE |
| K253739 | SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5…NKB · Traditional | Globus Medical, Inc. | 05/07/2026SE |
| K261130 | AccelFix Spinal Fixation SystemNKB · Special | L&K BIOMED Co., Ltd. | 05/05/2026SE |
More from L&K BIOMED Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K231098 | LineSider® Spinal SystemNKB · Traditional | 08/07/2023SE |
| K213355 | Toro-L Interbody Fusion SystemMAX · Traditional | 03/25/2022SE |
| K220453 | FlareHawk Interbody Fusion SystemMAX · Special | 03/24/2022SE |
| K212088 | Integrity Implants Navigated InstrumentsOLO · Traditional | 12/23/2021SE |
| K203038 | Toro-L Interbody Fusion SystemMAX · Traditional | 03/26/2021SE |
| K203367 | LineSider Spinal SystemNKB · Special | 12/03/2020SE |
| K202198 | FlareHawk Interbody Fusion SystemMAX · Traditional | 11/03/2020SE |
| K201367 | FlareHawk TiHawk9 Interbody Fusion SystemMAX · Traditional | 09/23/2020SE |
| K183184 | FlareHawk Interbody Fusion SystemMAX · Traditional | 04/03/2019SE |
| K182114 | FlareHawk Interbody Fusion SystemMAX · Traditional | 01/07/2019SE |
Questions and answers
When was LineSider Spinal System cleared by the FDA?
LineSider Spinal System (K190360) received a 510(k) decision of Substantially Equivalent on June 21, 2019, 126 days after the submission was received.
What is the product code of K190360?
The FDA product code is NKB – Thoracolumbosacral Pedicle Screw System, a Class II (moderate risk) device regulated under 21 CFR 888.3070.