AXIUM DETACHABLE COIL SYSTEM
K-Number: K081465 · 2008-08-19
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Device Summary
Frequently Asked Questions
What is the AXIUM DETACHABLE COIL SYSTEM?
AXIUM DETACHABLE COIL SYSTEM is a medical device that received FDA 510(k) clearance on 2008-08-19. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K081465.
When did AXIUM DETACHABLE COIL SYSTEM receive FDA 510(k) clearance?
AXIUM DETACHABLE COIL SYSTEM received FDA 510(k) clearance on 2008-08-19, under 510(k) number K081465.
Who is the listed applicant for AXIUM DETACHABLE COIL SYSTEM?
The FDA 510(k) record lists Micro Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXIUM DETACHABLE COIL SYSTEM?
The FDA product code for AXIUM DETACHABLE COIL SYSTEM is KRD.
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 Micro Therapeutics, 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: KRD)
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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