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FDA 510(k)

FEATHERLIFT EXTENDED LENGTH APTOS THREAD

K-Number: K041593 · 2004-09-20

Decision Date2004-09-20
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FEATHERLIFT EXTENDED LENGTH APTOS THREAD is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Specialties Corp. It received FDA 510(k) clearance on 2004-09-20 under 510(k) number K041593. 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 LENGTH APTOS THREAD?

FEATHERLIFT EXTENDED LENGTH APTOS THREAD is a medical device that received FDA 510(k) clearance on 2004-09-20. The listed applicant is Surgical Specialties Corp. The 510(k) number is K041593.

When did FEATHERLIFT EXTENDED LENGTH APTOS THREAD receive FDA 510(k) clearance?

FEATHERLIFT EXTENDED LENGTH APTOS THREAD received FDA 510(k) clearance on 2004-09-20, under 510(k) number K041593.

Who is the listed applicant for FEATHERLIFT EXTENDED LENGTH APTOS THREAD?

The FDA 510(k) record lists Surgical Specialties Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEATHERLIFT EXTENDED LENGTH APTOS THREAD?

The FDA product code for FEATHERLIFT EXTENDED LENGTH 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 Surgical Specialties Corp 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.

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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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