Universal Spinal System
FDA 510(k) K252729 · Double Medical Technology, Inc.
510(k) numberK252729
Submission
- Device name
- Universal Spinal System
- Applicant
- Double Medical Technology, Inc.
Xiamen, CN - Received
- August 28, 2025
- Decision date
- November 18, 2025
- 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.
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|---|---|---|---|
| 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.
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|---|---|---|
| K242348 | Locking Screw,CoCrMoHWC · Abbreviated | 12/04/2024SE |
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| K223753 | Cervical Plate SystemKWQ · Traditional | 03/14/2023SE |
| K221150 | Advanced Bone PlateHRS · Traditional | 01/25/2023SE |
| K221088 | Anatomic Bone PlateHRS · Traditional | 01/18/2023SE |
| K221090 | Metal Cannulated ScrewHWC · Traditional | 01/10/2023SE |
| K221221 | Advanced Intramedullary Nail SystemHSB · Traditional | 12/21/2022SE |
| K220921 | Metal Bone ScrewHWC · Traditional | 12/12/2022SE |
| K172830 | Double Medical Femoral Nail SystemHSB · Traditional | 08/24/2018SE |
| K172828 | Double Medical Cage SystemMAX · Traditional | 02/01/2018SE |
Questions and answers
When was Universal Spinal System cleared by the FDA?
Universal Spinal System (K252729) received a 510(k) decision of Substantially Equivalent on November 18, 2025, 82 days after the submission was received.
What is the product code of K252729?
The FDA product code is NKB – Thoracolumbosacral Pedicle Screw System, a Class II (moderate risk) device regulated under 21 CFR 888.3070.