ARIES Anterior Cervical Plate Systems
K-Number: K252776 · 2026-05-14
Device Summary
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. The listed applicant is ZheJiang Decans Medical Devices Co., Ltd.. The 510(k) number is K252776.
When did ARIES Anterior Cervical Plate Systems receive FDA 510(k) clearance?
ARIES Anterior Cervical Plate Systems received FDA 510(k) clearance on 2026-05-14, under 510(k) number K252776.
Who is the listed applicant for ARIES Anterior Cervical Plate Systems?
The FDA 510(k) record lists ZheJiang Decans Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARIES Anterior Cervical Plate Systems?
The FDA product code for ARIES Anterior Cervical Plate Systems is KWQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing ZheJiang Decans Medical Devices Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KWQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.