FDA 510(k)

TWIN FIX

K-Number: K022771 · 2002-09-23

Decision Date2002-09-23

Product CodeKTT

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TWIN FIX is the device name listed in this FDA 510(k) record. The listed applicant is Fixano SA. It received FDA 510(k) clearance on 2002-09-23 under 510(k) number K022771. 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 TWIN FIX?

TWIN FIX is a medical device that received FDA 510(k) clearance on 2002-09-23. The listed applicant is Fixano SA. The 510(k) number is K022771.

When did TWIN FIX receive FDA 510(k) clearance?

TWIN FIX received FDA 510(k) clearance on 2002-09-23, under 510(k) number K022771.

Who is the listed applicant for TWIN FIX?

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

What is the FDA product code for TWIN FIX?

The FDA product code for TWIN FIX is KTT.

Other records listing Fixano SA 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.

K023314MICROFIX K012062PF2 K012078RADIOFIX K012161FLEX-NAILS

Related Devices (Code: KTT)

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLC K260900DYNEX® External Fixation SystemsVilex, LLC K260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean Global K253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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.