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FDA 510(k)

EXTRAFIX EXTERNAL FIXATION SYSTEM

K-Number: K091258 · 2009-07-24

Decision Date2009-07-24
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXTRAFIX EXTERNAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Qfx Technologies, Inc.. It received FDA 510(k) clearance on 2009-07-24 under 510(k) number K091258. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTRAFIX EXTERNAL FIXATION SYSTEM?

EXTRAFIX EXTERNAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2009-07-24. The listed applicant is Qfx Technologies, Inc.. The 510(k) number is K091258.

When did EXTRAFIX EXTERNAL FIXATION SYSTEM receive FDA 510(k) clearance?

EXTRAFIX EXTERNAL FIXATION SYSTEM received FDA 510(k) clearance on 2009-07-24, under 510(k) number K091258.

Who is the listed applicant for EXTRAFIX EXTERNAL FIXATION SYSTEM?

The FDA 510(k) record lists Qfx Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTRAFIX EXTERNAL FIXATION SYSTEM?

The FDA product code for EXTRAFIX EXTERNAL FIXATION SYSTEM is KTT.

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.

Related Devices (Code: KTT)

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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