WINDOW CERVICAL DYNAMIC PLATE SYSTEM
K-Number: K993066 · 2000-06-07
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Device Summary
Frequently Asked Questions
What is the WINDOW CERVICAL DYNAMIC PLATE SYSTEM?
WINDOW CERVICAL DYNAMIC PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2000-06-07. The listed applicant is Advanced Spine Technology, Inc.. The 510(k) number is K993066.
When did WINDOW CERVICAL DYNAMIC PLATE SYSTEM receive FDA 510(k) clearance?
WINDOW CERVICAL DYNAMIC PLATE SYSTEM received FDA 510(k) clearance on 2000-06-07, under 510(k) number K993066.
Who is the listed applicant for WINDOW CERVICAL DYNAMIC PLATE SYSTEM?
The FDA 510(k) record lists Advanced Spine Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WINDOW CERVICAL DYNAMIC PLATE SYSTEM?
The FDA product code for WINDOW CERVICAL DYNAMIC 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 Advanced Spine Technology, 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.
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