KINETIC ANTERIOR CERVICAL PLATE
K-Number: K062643 · 2006-11-16
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Device Summary
Frequently Asked Questions
What is the KINETIC ANTERIOR CERVICAL PLATE?
KINETIC ANTERIOR CERVICAL PLATE is a medical device that received FDA 510(k) clearance on 2006-11-16. The listed applicant is Life Spine. The 510(k) number is K062643.
When did KINETIC ANTERIOR CERVICAL PLATE receive FDA 510(k) clearance?
KINETIC ANTERIOR CERVICAL PLATE received FDA 510(k) clearance on 2006-11-16, under 510(k) number K062643.
Who is the listed applicant for KINETIC ANTERIOR CERVICAL PLATE?
The FDA 510(k) record lists Life Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KINETIC ANTERIOR CERVICAL PLATE?
The FDA product code for KINETIC 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 Life 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.
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