ACTIVE ANTERIOR CERVICAL PLATE SYSTEM
K-Number: K073500 · 2008-07-03
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Device Summary
Frequently Asked Questions
What is the ACTIVE ANTERIOR CERVICAL PLATE SYSTEM?
ACTIVE ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-07-03. The listed applicant is Sanacor. The 510(k) number is K073500.
When did ACTIVE ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?
ACTIVE ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2008-07-03, under 510(k) number K073500.
Who is the listed applicant for ACTIVE ANTERIOR CERVICAL PLATE SYSTEM?
The FDA 510(k) record lists Sanacor as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACTIVE ANTERIOR CERVICAL PLATE SYSTEM?
The FDA product code for ACTIVE 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 Sanacor 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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