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FDA 510(k)

Orthex External Fixation System

K-Number: K223786 · 2023-02-10

ApplicantOrthoPediatrics Corp.
Decision Date2023-02-10
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Orthex External Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is OrthoPediatrics Corp.. It received FDA 510(k) clearance on 2023-02-10 under 510(k) number K223786. 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 Orthex External Fixation System?

Orthex External Fixation System is a medical device that received FDA 510(k) clearance on 2023-02-10. The listed applicant is OrthoPediatrics Corp.. The 510(k) number is K223786.

When did Orthex External Fixation System receive FDA 510(k) clearance?

Orthex External Fixation System received FDA 510(k) clearance on 2023-02-10, under 510(k) number K223786.

Who is the listed applicant for Orthex External Fixation System?

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

What is the FDA product code for Orthex External Fixation System?

The FDA product code for Orthex External Fixation System is KTT.

Other records listing OrthoPediatrics 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: 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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