FDA 510(k)

LINK Embrace Shoulder System - Reverse Configuration

K-번호: K231445 · 2023-11-16

결정일2023-11-16

제품 코드PHX

자문 위원회OR

결정Substantially Equivalent

기기 요약

LINK Embrace Shoulder System - Reverse Configuration is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 2023-11-16 under 510(k) number K231445. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the LINK Embrace Shoulder System - Reverse Configuration?

LINK Embrace Shoulder System - Reverse Configuration is a medical device that received FDA 510(k) clearance on 2023-11-16. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K231445.

When did LINK Embrace Shoulder System - Reverse Configuration receive FDA 510(k) clearance?

LINK Embrace Shoulder System - Reverse Configuration received FDA 510(k) clearance on 2023-11-16, under 510(k) number K231445.

Who is the listed applicant for LINK Embrace Shoulder System - Reverse Configuration?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINK Embrace Shoulder System - Reverse Configuration?

The FDA product code for LINK Embrace Shoulder System - Reverse Configuration is PHX.

Waldemar Link GmbH & Co. KG를 신청인으로 등재한 기타 기록

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