APOLLO Anterior Cervical Plate (ACP) System
FDA 510(k) K210325 · Aurora Spine, Inc.
510(k) numberK210325
Submission
- Device name
- APOLLO Anterior Cervical Plate (ACP) System
- Applicant
- Aurora Spine, Inc.
Carlsbad, CA, US - Received
- February 4, 2021
- Decision date
- March 23, 2021
- 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 |
|---|---|---|
| K243865 | AERO MIS Facet Fusion SystemMRW · Traditional | 03/24/2025SE |
| K221047 | SILO TFX MIS Sacroiliac Joint Fixation SystemOUR · Traditional | 10/03/2022SE |
| K221399 | ZIP MIS Interspinous Fusion SystemPEK · Traditional | 07/08/2022SE |
| K220610 | Solo-LOVD · Traditional | 05/27/2022SE |
| K210521 | DEXA-C Cervical Interbody SystemODP · Traditional | 08/02/2021SE |
| K141317 | Zip Mis Interspinous Fusion SystemPEK · Traditional | 11/17/2014SE |
| K140715 | Zip Mis Interspinous Fusion SystemPEK · Special | 04/17/2014SE |
| K133967 | Interbody Cage SystemMAX · Traditional | 01/31/2014SE |
| K133091 | Zip Mis Interspinous Fusion SystemPEK · Traditional | 11/27/2013SE |
Questions and answers
When was APOLLO Anterior Cervical Plate (ACP) System cleared by the FDA?
APOLLO Anterior Cervical Plate (ACP) System (K210325) received a 510(k) decision of Substantially Equivalent on March 23, 2021, 47 days after the submission was received.
What is the product code of K210325?
The FDA product code is KWQ – Appliance, Fixation, Spinal Intervertebral Body, a Class II (moderate risk) device regulated under 21 CFR 888.3060.