FDA 510(k)

Triathlon® 全膝关节系统 - Triathlon® X3® 内侧稳定胫骨假体植入物

K号: K253637 · 2026-02-18

申请人Howmedica Osteonics Corp., Dba Stryker Orthopaedics

决定日期2026-02-18

产品代码MBH

咨询委员会OR 请注意，由于原文中未提供具体的医疗设备监管文本，以下是一个示例翻译，您可以根据实际文本进行调整： --- 产品名称：[产品名称] 公司名称：[公司名称] 根据FDA 510(k)预市场批准程序，[产品名称]已获得批准，用于[产品用途描述]。产品注册号：[注册号] PMA编号：[PMA编号] 临床试验编号（NCT）：[NCT编号] PubMed ID（PMID）：[PMID编号] 更多信息请访问以下链接： [URL] --- 请将上述示例中的[产品名称]、[公司名称]、[注册号]、[PMA编号]、[NCT编号]、[PMID编号]和[URL]替换为实际的文本内容。

决定实质等同

器械摘要

Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2026-02-18 under 510(k) number K253637. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert?

Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert is a medical device that received FDA 510(k) clearance on 2026-02-18. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K253637.

When did Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert receive FDA 510(k) clearance?

Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert received FDA 510(k) clearance on 2026-02-18, under 510(k) number K253637.

Who is the listed applicant for Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert?

The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert?

The FDA product code for Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert is MBH.

列明Howmedica Osteonics Corp., Dba Stryker Orthopaedics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。

K261898Triathlon® 膝关节系统；Triathlon® 活动铰链膝关节系统；Scorpio® 全膝关节系统 K261624Omnifit® 20°系列I插入件；Omnifit® Crossfire® 10°系列II插入件；限制性髋臼插入件；Trident® Crossfire® 0°聚乙烯插入件；Trident® Crossfire® 10°聚乙烯插入件；System 12 Crossfire® 10°插入件；Trident® 0°限制性髋臼插入件；Trident® 限制性髋臼衬垫；Trident® 全聚乙烯限制性髋臼插入件；Crossfire® 异心插入件10°；Artisan® 骨塞；UHR® 通用头双极组件 K252898Triathlon® Tritanium® 非对称髌骨；Triathlon® 对称髌骨；Triathlon® 对称髌骨；Triathlon® 非对称髌骨；Scorpio® 通用穹顶髌骨；Triathlon® 螺旋防撞垫 K252044铁人三项® 全膝关节系统 - 铁人三项® 金色股骨组件 K251665铁人三项®铰链膝关节系统 K250989Stryker 和 Serf 髋关节设备

查看所有 27 个设备 →

官方来源

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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。