Equinoxe® 肱骨重建假体;Equinoxe® 无柄肩关节植入物
K号: K250713 · 2025-12-01
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器械摘要
常见问题
What is the Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants?
Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants is a medical device that received FDA 510(k) clearance on 2025-12-01. The listed applicant is Exactech, Inc.. The 510(k) number is K250713.
When did Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants receive FDA 510(k) clearance?
Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants received FDA 510(k) clearance on 2025-12-01, under 510(k) number K250713.
Who is the listed applicant for Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants?
The FDA 510(k) record lists Exactech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants?
The FDA product code for Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder Implants is KWT.
相关临床试验
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列明Exactech, Inc.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:KWT)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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