FEATHERLIFT EXTENDED APTOS THREAD
K-Number: K043591 · 2005-03-04
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Device Summary
Frequently Asked Questions
What is the FEATHERLIFT EXTENDED APTOS THREAD?
FEATHERLIFT EXTENDED APTOS THREAD is a medical device that received FDA 510(k) clearance on 2005-03-04. The listed applicant is Kmi Kolster Methods, Inc.. The 510(k) number is K043591.
When did FEATHERLIFT EXTENDED APTOS THREAD receive FDA 510(k) clearance?
FEATHERLIFT EXTENDED APTOS THREAD received FDA 510(k) clearance on 2005-03-04, under 510(k) number K043591.
Who is the listed applicant for FEATHERLIFT EXTENDED APTOS THREAD?
The FDA 510(k) record lists Kmi Kolster Methods, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FEATHERLIFT EXTENDED APTOS THREAD?
The FDA product code for FEATHERLIFT EXTENDED APTOS THREAD is GAW.
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 Kmi Kolster Methods, 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: GAW)
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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