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FDA 510(k)

FEATHERLIFT EXTENDED APTOS THREAD

K-Number: K043591 · 2005-03-04

Decision Date2005-03-04
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FEATHERLIFT EXTENDED APTOS THREAD is the device name listed in this FDA 510(k) record. The listed applicant is Kmi Kolster Methods, Inc.. It received FDA 510(k) clearance on 2005-03-04 under 510(k) number K043591. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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