FDA 510(k)

Flex-Thread™尺骨中骨髓内釘システム

K番号: K222390 · 2022-11-21

申請者Flower Orthopedics Corporation Dba Conventus Flower

決定日2022-11-21

製品コードHSB

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OR [翻訳] OR 注：原文が具体的な内容を含んでいないため、翻訳は単なる「OR」のままです。

決定Substantially Equivalent

医療機器の概要

Flex-Thread™ Ulna Intramedullary Nail System is the device name listed in this FDA 510(k) record. The listed applicant is Flower Orthopedics Corporation Dba Conventus Flower. It received FDA 510(k) clearance on 2022-11-21 under 510(k) number K222390. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Flex-Thread™ Ulna Intramedullary Nail System?

Flex-Thread™ Ulna Intramedullary Nail System is a medical device that received FDA 510(k) clearance on 2022-11-21. The listed applicant is Flower Orthopedics Corporation Dba Conventus Flower. The 510(k) number is K222390.

When did Flex-Thread™ Ulna Intramedullary Nail System receive FDA 510(k) clearance?

Flex-Thread™ Ulna Intramedullary Nail System received FDA 510(k) clearance on 2022-11-21, under 510(k) number K222390.

Who is the listed applicant for Flex-Thread™ Ulna Intramedullary Nail System?

The FDA 510(k) record lists Flower Orthopedics Corporation Dba Conventus Flower as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Flex-Thread™ Ulna Intramedullary Nail System?

The FDA product code for Flex-Thread™ Ulna Intramedullary Nail System is HSB.

申請者としてFlower Orthopedics Corporation Dba Conventus Flowerを記載するその他の記録

K212030Flex-Thread™遠位fibula内骨髄釘システム

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