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FDA 510(k)

Omni Foot and Ankle Plating System

K-Number: K221362 · 2022-06-10

ApplicantExremity Medical, LLC
Decision Date2022-06-10
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Omni Foot and Ankle Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Exremity Medical, LLC. It received FDA 510(k) clearance on 2022-06-10 under 510(k) number K221362. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Omni Foot and Ankle Plating System?

Omni Foot and Ankle Plating System is a medical device that received FDA 510(k) clearance on 2022-06-10. The listed applicant is Exremity Medical, LLC. The 510(k) number is K221362.

When did Omni Foot and Ankle Plating System receive FDA 510(k) clearance?

Omni Foot and Ankle Plating System received FDA 510(k) clearance on 2022-06-10, under 510(k) number K221362.

Who is the listed applicant for Omni Foot and Ankle Plating System?

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

What is the FDA product code for Omni Foot and Ankle Plating System?

The FDA product code for Omni Foot and Ankle Plating System is HRS.

Related Devices (Code: HRS)

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.

K260277MIKRON TRAUMA BONE PLATE& SCREW SYSTEMMikron Makina San. ve Tic. Ltd. Sti.K261511Xpert AnkleNewclip TechnicsK261406Versalock Proximal Tibial Plating SystemGM Dos Reis Industria e Comercio Ltda.K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB )TriMed, Inc.K261191Alians Elbow SNewclip TechnicsK261054RibPlate SystemStryker Leibinger GmbH & Co KG

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.

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