ARIES Anterior Cervical Plate Systems
K-Number: K252776 · 2026-05-14
Decision Date2026-05-14
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
ARIES Anterior Cervical Plate Systems is a medical device manufactured by ZheJiang Decans Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2026-05-14 under approval number K252776. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ARIES Anterior Cervical Plate Systems?
ARIES Anterior Cervical Plate Systems is a medical device that received FDA 510(k) clearance on 2026-05-14. It is manufactured by ZheJiang Decans Medical Devices Co., Ltd.. The 510(k) number is K252776.
When was ARIES Anterior Cervical Plate Systems approved by the FDA?
ARIES Anterior Cervical Plate Systems received FDA 510(k) clearance on 2026-05-14, under approval number K252776.
What company makes ARIES Anterior Cervical Plate Systems?
ARIES Anterior Cervical Plate Systems is manufactured by ZheJiang Decans Medical Devices Co., Ltd..
What is the FDA product code for ARIES Anterior Cervical Plate Systems?
The FDA product code for ARIES Anterior Cervical Plate Systems is KWQ.
Other Devices by ZheJiang Decans Medical Devices Co., Ltd.
Related Devices (Code: KWQ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.