SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline System
FDA 510(k) K253739 · Globus Medical, Inc.
510(k) numberK253739
Submission
- Device name
- SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline System
- Applicant
- Globus Medical, Inc.
Audubon, PA, US - Received
- November 24, 2025
- Decision date
- May 7, 2026
- 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 |
| K261130 | AccelFix Spinal Fixation SystemNKB · Special | L&K BIOMED Co., Ltd. | 05/05/2026SE |
| K253966 | PERLA® TL Posterior Thoraco-lumbar Fixation SystemNKB · Traditional | Spineart SA | 05/01/2026SE |
More from Spineart SA
| 510(k) | Device | Decision |
|---|---|---|
| K254043 | TRIVANCE Hip StemLPH · Traditional | 08/04/2026SE |
| K262251 | ACTIFY Total Knee System, ACTIFY 3D Total Knee System (ACTIFY MC Tibial Insert)JWH · Special | 07/31/2026SE |
| K253401 | SCRIPT Implant SystemOVD · Traditional | 04/29/2026SE |
| K261043 | AUTOBAHN Nailing SystemHSB · Special | 04/24/2026SE |
| K252166 | RIB LINK Fixation SystemHRS · Traditional | 02/26/2026SE |
| K253876 | HEDRON Cervical Spacers (HEDRON C-MIS Spacer)OVE · Special | 12/22/2025SE |
| K250599 | ExcelsiusGPS InstrumentsOLO · Traditional | 11/05/2025SE |
| K251161 | ANTHEM® Fracture SystemHRS · Traditional | 08/18/2025SE |
| K241525 | ExcelsiusXRSBF · Traditional | 07/08/2025SE |
| K243456 | ONVOY Acetabular SystemLPH · Traditional | 06/06/2025SE |
Questions and answers
When was SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline System cleared by the FDA?
SCRIPT Rods, CREO Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline System (K253739) received a 510(k) decision of Substantially Equivalent on May 7, 2026, 164 days after the submission was received.
What is the product code of K253739?
The FDA product code is NKB – Thoracolumbosacral Pedicle Screw System, a Class II (moderate risk) device regulated under 21 CFR 888.3070.