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FDA 510(k)

SIDEKICK RAIL FIXATOR

K-Number: K080071 · 2008-02-07

ApplicantWrightmedicaltechnologyinc
Decision Date2008-02-07
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SIDEKICK RAIL FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2008-02-07 under 510(k) number K080071. 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 SIDEKICK RAIL FIXATOR?

SIDEKICK RAIL FIXATOR is a medical device that received FDA 510(k) clearance on 2008-02-07. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K080071.

When did SIDEKICK RAIL FIXATOR receive FDA 510(k) clearance?

SIDEKICK RAIL FIXATOR received FDA 510(k) clearance on 2008-02-07, under 510(k) number K080071.

Who is the listed applicant for SIDEKICK RAIL FIXATOR?

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

What is the FDA product code for SIDEKICK RAIL FIXATOR?

The FDA product code for SIDEKICK RAIL FIXATOR is KTT.

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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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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