Skyway Anterior Cervical Plate System
K-Number: K243015 · 2024-11-05
Device Summary
Frequently Asked Questions
What is the Skyway Anterior Cervical Plate System?
Skyway Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2024-11-05. The listed applicant is Kyocera Medical Technologies, Inc.. The 510(k) number is K243015.
When did Skyway Anterior Cervical Plate System receive FDA 510(k) clearance?
Skyway Anterior Cervical Plate System received FDA 510(k) clearance on 2024-11-05, under 510(k) number K243015.
Who is the listed applicant for Skyway Anterior Cervical Plate System?
The FDA 510(k) record lists Kyocera Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Skyway Anterior Cervical Plate System?
The FDA product code for Skyway Anterior Cervical Plate System 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 Kyocera Medical Technologies, Inc. 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.