COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM
K-Number: K955365 · 1996-03-27
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Device Summary
Frequently Asked Questions
What is the COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM?
COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Sofamor Danek USA,Inc.. The 510(k) number is K955365.
When did COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM receive FDA 510(k) clearance?
COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM received FDA 510(k) clearance on 1996-03-27, under 510(k) number K955365.
Who is the listed applicant for COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM?
The FDA 510(k) record lists Sofamor Danek USA,Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM?
The FDA product code for COMPACT COTREL-DUBOUSSET (CCD) SPINAL SYSTEM is KWP.
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 Sofamor Danek USA,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: KWP)
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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