Synthes Matrix System
FDA 510(k) K120928 · Synthes Spine
510(k) numberK120928
Submission
- Device name
- Synthes Matrix System
- Applicant
- Synthes Spine
West Chester, PA, US - Received
- March 27, 2012
- Decision date
- May 18, 2012
- 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 |
|---|---|---|
| K122211 | Synthes Navigable Pedicle Preparation InstrumentsHAW · Traditional | 12/17/2012SE |
| K120838 | Synthes Matrix SystemNKB · Traditional | 07/31/2012SE |
| K121852 | Synthes Zero-P Variable Angle (Va)OVE · Special | 07/25/2012SE |
| K111048 | Synthes Scout Tack FixationOMR · Traditional | 06/14/2012SESU |
| K120571 | Synthes Uss ConnectorNKB · Traditional | 05/14/2012SE |
| K113149 | Synthes Uss ConnectorsMNI · Traditional | 02/01/2012SE |
| K113044 | Synthes MirsNKB · Traditional | 12/21/2011SE |
| K112459 | Synthes Zero-POVE · Special | 12/12/2011SE |
| K111358 | Synthes UssNKB · Traditional | 11/18/2011SE |
| K112068 | Synthes Zero-P Variable Angle (Va)OVE · Traditional | 11/07/2011SE |
Questions and answers
When was Synthes Matrix System cleared by the FDA?
Synthes Matrix System (K120928) received a 510(k) decision of Substantially Equivalent on May 18, 2012, 52 days after the submission was received.
What is the product code of K120928?
The FDA product code is NKB – Thoracolumbosacral Pedicle Screw System, a Class II (moderate risk) device regulated under 21 CFR 888.3070.