Liberty Anterior Cervical Plate
K-Number: K172585 · 2017-10-23
Device Summary
Frequently Asked Questions
What is the Liberty Anterior Cervical Plate?
Liberty Anterior Cervical Plate is a medical device that received FDA 510(k) clearance on 2017-10-23. The listed applicant is Valorus Spine. The 510(k) number is K172585.
When did Liberty Anterior Cervical Plate receive FDA 510(k) clearance?
Liberty Anterior Cervical Plate received FDA 510(k) clearance on 2017-10-23, under 510(k) number K172585.
Who is the listed applicant for Liberty Anterior Cervical Plate?
The FDA 510(k) record lists Valorus Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Liberty Anterior Cervical Plate?
The FDA product code for Liberty Anterior Cervical Plate 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 Valorus Spine 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.