Velox Anterior Cervical Plate System
FDA 510(k) K131521 · Spinecraft, LLC
510(k) numberK131521
Submission
- Device name
- Velox Anterior Cervical Plate System
- Applicant
- Spinecraft, LLC
Westmont, IL, US - Received
- May 28, 2013
- Decision date
- December 24, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWQ – Appliance, Fixation, Spinal Intervertebral Body
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3060
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KWQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261309 | Palisades Buttress Plate SystemKWQ · Traditional | Bethesda Medical Devices, LLC | 07/16/2026SE |
| K252776 | ARIES Anterior Cervical Plate SystemsKWQ · Traditional | ZheJiang Decans Medical Devices Co., Ltd. | 05/14/2026SE |
| K261112 | CastleLoc-P Anterior Cervical Plate SystemKWQ · Special | L&K BIOMED Co., Ltd. | 05/06/2026SE |
| K260570 | corra cervical plating systemKWQ · Traditional | Carlsmed, Inc. | 04/22/2026SE |
| K260697 | VyPlate Anterior Cervical Plate SystemKWQ · Special | Vy Spine, LLC | 03/27/2026SE |
| K260015 | ANTERIS Thoracolumbar Plate SystemKWQ · Traditional | SpineCraft | 03/04/2026SE |
| K251940 | PathLoc Lumbar Plate SystemKWQ · Traditional | L&K BIOMED Co., Ltd. | 03/03/2026SE |
| K254182 | AsterKWQ · Traditional | Osteonic Co., Ltd. | 02/26/2026SE |
| K253201 | Lumbar Spine Truss System - Plating Solution (LSTS-PS)KWQ · Special | 4Web, Inc. | 02/12/2026SE |
| K252611 | aprevo® cervical plating systemKWQ · Traditional | Carlsmed, Inc. | 12/22/2025SE |
More from Carlsmed, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K253260 | ORIO-3D Cage SystemODP · Traditional | 04/16/2026SE |
| K260015 | ANTERIS Thoracolumbar Plate SystemKWQ · Traditional | 03/04/2026SE |
| K223301 | ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments SystemOLO · Traditional | 07/20/2023SE |
| K223273 | ASTRA Spine SystemNKB · Traditional | 12/22/2022SE |
| K211935 | ORIO-Ti Intervertebral Body Fusion Cage SystemODP · Traditional | 09/30/2021SE |
| K211323 | ASTRA Spine SystemNKB · Special | 06/03/2021SE |
| K181350 | ASTRA-OCT Spine SystemNKG · Traditional | 07/06/2018SE |
| K143683 | APEX-DL Spine SystemNKB · Traditional | 05/22/2015SE |
| K150417 | Astra Spine SystemNKB · Traditional | 05/19/2015SE |
| K132603 | Apex Spine SystemNKB · Traditional | 11/20/2013SE |
Questions and answers
When was Velox Anterior Cervical Plate System cleared by the FDA?
Velox Anterior Cervical Plate System (K131521) received a 510(k) decision of Substantially Equivalent on December 24, 2013, 210 days after the submission was received.
What is the product code of K131521?
The FDA product code is KWQ – Appliance, Fixation, Spinal Intervertebral Body, a Class II (moderate risk) device regulated under 21 CFR 888.3060.