KING COBRA ANTERIOR CERVICAL PLATE
K-Number: K103068 · 2011-01-14
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Device Summary
Frequently Asked Questions
What is the KING COBRA ANTERIOR CERVICAL PLATE?
KING COBRA ANTERIOR CERVICAL PLATE is a medical device that received FDA 510(k) clearance on 2011-01-14. The listed applicant is Eminent Spine. The 510(k) number is K103068.
When did KING COBRA ANTERIOR CERVICAL PLATE receive FDA 510(k) clearance?
KING COBRA ANTERIOR CERVICAL PLATE received FDA 510(k) clearance on 2011-01-14, under 510(k) number K103068.
Who is the listed applicant for KING COBRA ANTERIOR CERVICAL PLATE?
The FDA 510(k) record lists Eminent Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KING COBRA ANTERIOR CERVICAL PLATE?
The FDA product code for KING COBRA 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 Eminent 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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