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FDA 510(k)

EXTERNAL FIXATION RING

K-Number: K022423 · 2002-09-17

ApplicantRigid FX Orthopedics, Incorporated
Decision Date2002-09-17
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXTERNAL FIXATION RING is the device name listed in this FDA 510(k) record. The listed applicant is Rigid FX Orthopedics, Incorporated. It received FDA 510(k) clearance on 2002-09-17 under 510(k) number K022423. 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 EXTERNAL FIXATION RING?

EXTERNAL FIXATION RING is a medical device that received FDA 510(k) clearance on 2002-09-17. The listed applicant is Rigid FX Orthopedics, Incorporated. The 510(k) number is K022423.

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

EXTERNAL FIXATION RING received FDA 510(k) clearance on 2002-09-17, under 510(k) number K022423.

Who is the listed applicant for EXTERNAL FIXATION RING?

The FDA 510(k) record lists Rigid FX Orthopedics, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTERNAL FIXATION RING?

The FDA product code for EXTERNAL FIXATION RING 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.

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Other records listing Rigid FX Orthopedics, Incorporated 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.

K020311CLEARVIEW WRIST FIXATOR

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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