IST ANTERIOR CERVICAL PLATE SYSTEM
K-Number: K072650 · 2007-11-28
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Device Summary
Frequently Asked Questions
What is the IST ANTERIOR CERVICAL PLATE SYSTEM?
IST ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-28. The listed applicant is Innovative Spinal Technologies, Inc.. The 510(k) number is K072650.
When did IST ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?
IST ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2007-11-28, under 510(k) number K072650.
Who is the listed applicant for IST ANTERIOR CERVICAL PLATE SYSTEM?
The FDA 510(k) record lists Innovative Spinal Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IST ANTERIOR CERVICAL PLATE SYSTEM?
The FDA product code for IST 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 Innovative Spinal Technologies, 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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