OvertureTi膝关节表面重塑系统™
K号: K242746 · 2024-10-07
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决定日期2024-10-07
产品代码HSX
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：
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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]
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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
OvertureTi Knee Resurfacing SystemTM is the device name listed in this FDA 510(k) record. The listed applicant is Overture Orthopaedics. It received FDA 510(k) clearance on 2024-10-07 under 510(k) number K242746. The device is classified under product code HSX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the OvertureTi Knee Resurfacing SystemTM?
OvertureTi Knee Resurfacing SystemTM is a medical device that received FDA 510(k) clearance on 2024-10-07. The listed applicant is Overture Orthopaedics. The 510(k) number is K242746.
When did OvertureTi Knee Resurfacing SystemTM receive FDA 510(k) clearance?
OvertureTi Knee Resurfacing SystemTM received FDA 510(k) clearance on 2024-10-07, under 510(k) number K242746.
Who is the listed applicant for OvertureTi Knee Resurfacing SystemTM?
The FDA 510(k) record lists Overture Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OvertureTi Knee Resurfacing SystemTM?
The FDA product code for OvertureTi Knee Resurfacing SystemTM is HSX.
相关临床试验
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：HSX）
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。
K261609自由部分膝关节系统Maxx Orthopedics, Inc.K260796Tahoe Unicondylar 关节系统，带 TiNbN 涂层Shalby Advanced Technologies, Inc. Dba Consensus OrthopedicsK251771Cambridge 部分膝关节Signature Orthopaedics Pty, Ltd.K251834Persona部分膝关节Zimmer BiometK251618MOTO 部分膝关节系统扩展Medacta International S.A.K251453Arthrex iBalance Partial Knee SystemArthrex, Inc.
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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